Genetics: The branch of science concerned with the means and consequences of transmission and generation of the components of biological inheritance. (Stedman, 26th ed)Genetics, Population: The discipline studying genetic composition of populations and effects of factors such as GENETIC SELECTION, population size, MUTATION, migration, and GENETIC DRIFT on the frequencies of various GENOTYPES and PHENOTYPES using a variety of GENETIC TECHNIQUES.Genetics, Behavioral: The experimental study of the relationship between the genotype of an organism and its behavior. The scope includes the effects of genes on simple sensory processes to complex organization of the nervous system.Molecular Biology: A discipline concerned with studying biological phenomena in terms of the chemical and physical interactions of molecules.Genetic Variation: Genotypic differences observed among individuals in a population.Phenotype: The outward appearance of the individual. It is the product of interactions between genes, and between the GENOTYPE and the environment.Genetic Predisposition to Disease: A latent susceptibility to disease at the genetic level, which may be activated under certain conditions.Genetic Testing: Detection of a MUTATION; GENOTYPE; KARYOTYPE; or specific ALLELES associated with genetic traits, heritable diseases, or predisposition to a disease, or that may lead to the disease in descendants. It includes prenatal genetic testing.Genetic Counseling: An educational process that provides information and advice to individuals or families about a genetic condition that may affect them. The purpose is to help individuals make informed decisions about marriage, reproduction, and other health management issues based on information about the genetic disease, the available diagnostic tests, and management programs. Psychosocial support is usually offered.Models, Genetic: Theoretical representations that simulate the behavior or activity of genetic processes or phenomena. They include the use of mathematical equations, computers, and other electronic equipment.Mutation: Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations.Genotype: The genetic constitution of the individual, comprising the ALLELES present at each GENETIC LOCUS.Chromosome Mapping: Any method used for determining the location of and relative distances between genes on a chromosome.Genetic Services: Organized services to provide diagnosis, treatment, and prevention of genetic disorders.Genetic Linkage: The co-inheritance of two or more non-allelic GENES due to their being located more or less closely on the same CHROMOSOME.Genetic Research: Research into the cause, transmission, amelioration, elimination, or enhancement of inherited disorders and traits.Genome-Wide Association Study: An analysis comparing the allele frequencies of all available (or a whole GENOME representative set of) polymorphic markers in unrelated patients with a specific symptom or disease condition, and those of healthy controls to identify markers associated with a specific disease or condition.Alleles: Variant forms of the same gene, occupying the same locus on homologous CHROMOSOMES, and governing the variants in production of the same gene product.Quantitative Trait Loci: Genetic loci associated with a QUANTITATIVE TRAIT.Genomics: The systematic study of the complete DNA sequences (GENOME) of organisms.Polymorphism, Single Nucleotide: A single nucleotide variation in a genetic sequence that occurs at appreciable frequency in the population.Genetic Markers: A phenotypically recognizable genetic trait which can be used to identify a genetic locus, a linkage group, or a recombination event.Eugenics: The attempt to improve the PHENOTYPES of future generations of the human population by fostering the reproduction of those with favorable phenotypes and GENOTYPES and hampering or preventing BREEDING by those with "undesirable" phenotypes and genotypes. The concept is largely discredited. (McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)Genetic Diseases, Inborn: Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.Genetic Techniques: Chromosomal, biochemical, intracellular, and other methods used in the study of genetics.Microsatellite Repeats: A variety of simple repeat sequences that are distributed throughout the GENOME. They are characterized by a short repeat unit of 2-8 basepairs that is repeated up to 100 times. They are also known as short tandem repeats (STRs).Selection, Genetic: Differential and non-random reproduction of different genotypes, operating to alter the gene frequencies within a population.Crosses, Genetic: Deliberate breeding of two different individuals that results in offspring that carry part of the genetic material of each parent. The parent organisms must be genetically compatible and may be from different varieties or closely related species.Biological Evolution: The process of cumulative change over successive generations through which organisms acquire their distinguishing morphological and physiological characteristics.Polymorphism, Genetic: The regular and simultaneous occurrence in a single interbreeding population of two or more discontinuous genotypes. The concept includes differences in genotypes ranging in size from a single nucleotide site (POLYMORPHISM, SINGLE NUCLEOTIDE) to large nucleotide sequences visible at a chromosomal level.Sequence Analysis, DNA: A multistage process that includes cloning, physical mapping, subcloning, determination of the DNA SEQUENCE, and information analysis.Evolution, Molecular: The process of cumulative change at the level of DNA; RNA; and PROTEINS, over successive generations.Molecular Sequence Data: Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.Forensic Genetics: The application of genetic analyses and MOLECULAR DIAGNOSTIC TECHNIQUES to legal matters and crime analysis.Quantitative Trait, Heritable: A characteristic showing quantitative inheritance such as SKIN PIGMENTATION in humans. (From A Dictionary of Genetics, 4th ed)Inheritance Patterns: The different ways GENES and their ALLELES interact during the transmission of genetic traits that effect the outcome of GENE EXPRESSION.Phylogeny: The relationships of groups of organisms as reflected by their genetic makeup.Genome, Human: The complete genetic complement contained in the DNA of a set of CHROMOSOMES in a HUMAN. The length of the human genome is about 3 billion base pairs.Genetic Loci: Specific regions that are mapped within a GENOME. Genetic loci are usually identified with a shorthand notation that indicates the chromosome number and the position of a specific band along the P or Q arm of the chromosome where they are found. For example the locus 6p21 is found within band 21 of the P-arm of CHROMOSOME 6. Many well known genetic loci are also known by common names that are associated with a genetic function or HEREDITARY DISEASE.Gene Frequency: The proportion of one particular in the total of all ALLELES for one genetic locus in a breeding POPULATION.Species Specificity: The restriction of a characteristic behavior, anatomical structure or physical system, such as immune response; metabolic response, or gene or gene variant to the members of one species. It refers to that property which differentiates one species from another but it is also used for phylogenetic levels higher or lower than the species.Pedigree: The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition.Epistasis, Genetic: A form of gene interaction whereby the expression of one gene interferes with or masks the expression of a different gene or genes. Genes whose expression interferes with or masks the effects of other genes are said to be epistatic to the effected genes. Genes whose expression is affected (blocked or masked) are hypostatic to the interfering genes.Human Genome Project: A coordinated effort of researchers to map (CHROMOSOME MAPPING) and sequence (SEQUENCE ANALYSIS, DNA) the human GENOME.Genetic Association Studies: The analysis of a sequence such as a region of a chromosome, a haplotype, a gene, or an allele for its involvement in controlling the phenotype of a specific trait, metabolic pathway, or disease.Pharmacogenetics: A branch of genetics which deals with the genetic variability in individual responses to drugs and drug metabolism (BIOTRANSFORMATION).Haplotypes: The genetic constitution of individuals with respect to one member of a pair of allelic genes, or sets of genes that are closely linked and tend to be inherited together such as those of the MAJOR HISTOCOMPATIBILITY COMPLEX.Environment: The external elements and conditions which surround, influence, and affect the life and development of an organism or population.Databases, Genetic: Databases devoted to knowledge about specific genes and gene products.Developmental Biology: The field of biology which deals with the process of the growth and differentiation of an organism.Base Sequence: The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence.Genetic Determinism: The theory that human CHARACTER and BEHAVIOR are shaped by the GENES that comprise the individual's GENOTYPE rather than by CULTURE; ENVIRONMENT; and individual choice.Genetic Privacy: The protection of genetic information about an individual, family, or population group, from unauthorized disclosure.Gene-Environment Interaction: The combined effects of genotypes and environmental factors together on phenotypic characteristics.Recombination, Genetic: Production of new arrangements of DNA by various mechanisms such as assortment and segregation, CROSSING OVER; GENE CONVERSION; GENETIC TRANSFORMATION; GENETIC CONJUGATION; GENETIC TRANSDUCTION; or mixed infection of viruses.Linkage Disequilibrium: Nonrandom association of linked genes. This is the tendency of the alleles of two separate but already linked loci to be found together more frequently than would be expected by chance alone.History, 20th Century: Time period from 1901 through 2000 of the common era.Genetics, Microbial: A subdiscipline of genetics which deals with the genetic mechanisms and processes of microorganisms.Genetic Phenomena: The processes, properties and biological objects that are involved in maintaining, expressing, and transmitting from one organism to another, genetically encoded traits.Multifactorial Inheritance: A phenotypic outcome (physical characteristic or disease predisposition) that is determined by more than one gene. Polygenic refers to those determined by many genes, while oligogenic refers to those determined by a few genes.Hybridization, Genetic: The genetic process of crossbreeding between genetically dissimilar parents to produce a hybrid.Genome: The genetic complement of an organism, including all of its GENES, as represented in its DNA, or in some cases, its RNA.Gene Flow: The change in gene frequency in a population due to migration of gametes or individuals (ANIMAL MIGRATION) across population barriers. In contrast, in GENETIC DRIFT the cause of gene frequency changes are not a result of population or gamete movement.Heterozygote: An individual having different alleles at one or more loci regarding a specific character.Drosophila: A genus of small, two-winged flies containing approximately 900 described species. These organisms are the most extensively studied of all genera from the standpoint of genetics and cytology.Breeding: The production of offspring by selective mating or HYBRIDIZATION, GENETIC in animals or plants.Genes, Plant: The functional hereditary units of PLANTS.Drosophila melanogaster: A species of fruit fly much used in genetics because of the large size of its chromosomes.DNA, Plant: Deoxyribonucleic acid that makes up the genetic material of plants.DNA, Mitochondrial: Double-stranded DNA of MITOCHONDRIA. In eukaryotes, the mitochondrial GENOME is circular and codes for ribosomal RNAs, transfer RNAs, and about 10 proteins.Genome, Plant: The genetic complement of a plant (PLANTS) as represented in its DNA.Genetic Heterogeneity: The presence of apparently similar characters for which the genetic evidence indicates that different genes or different genetic mechanisms are involved in different pedigrees. In clinical settings genetic heterogeneity refers to the presence of a variety of genetic defects which cause the same disease, often due to mutations at different loci on the same gene, a finding common to many human diseases including ALZHEIMER DISEASE; CYSTIC FIBROSIS; LIPOPROTEIN LIPASE DEFICIENCY, FAMILIAL; and POLYCYSTIC KIDNEY DISEASES. (Rieger, et al., Glossary of Genetics: Classical and Molecular, 5th ed; Segen, Dictionary of Modern Medicine, 1992)Models, Biological: Theoretical representations that simulate the behavior or activity of biological processes or diseases. For disease models in living animals, DISEASE MODELS, ANIMAL is available. Biological models include the use of mathematical equations, computers, and other electronic equipment.History, 21st Century: Time period from 2001 through 2100 of the common era.Computational Biology: A field of biology concerned with the development of techniques for the collection and manipulation of biological data, and the use of such data to make biological discoveries or predictions. This field encompasses all computational methods and theories for solving biological problems including manipulation of models and datasets.Software: Sequential operating programs and data which instruct the functioning of a digital computer.Geography: The science dealing with the earth and its life, especially the description of land, sea, and air and the distribution of plant and animal life, including humanity and human industries with reference to the mutual relations of these elements. (From Webster, 3d ed)Genetic Engineering: Directed modification of the gene complement of a living organism by such techniques as altering the DNA, substituting genetic material by means of a virus, transplanting whole nuclei, transplanting cell hybrids, etc.Individualized Medicine: Therapeutic approach tailoring therapy for genetically defined subgroups of patients.Heredity: The transmission of traits encoded in GENES from parent to offspring.Disease Models, Animal: Naturally occurring or experimentally induced animal diseases with pathological processes sufficiently similar to those of human diseases. They are used as study models for human diseases.Reproduction: The total process by which organisms produce offspring. (Stedman, 25th ed)Genetic Speciation: The splitting of an ancestral species into daughter species that coexist in time (King, Dictionary of Genetics, 6th ed). Causal factors may include geographic isolation, HABITAT geometry, migration, REPRODUCTIVE ISOLATION, random GENETIC DRIFT and MUTATION.Endophenotypes: Measurable biological (physiological, biochemical, and anatomical features), behavioral (psychometric pattern) or cognitive markers that are found more often in individuals with a disease than in the general population. Because many endophenotypes are present before the disease onset and in individuals with heritable risk for disease such as unaffected family members, they can be used to help diagnose and search for causative genes.Inbreeding: The mating of plants or non-human animals which are closely related genetically.Genetic Drift: The fluctuation of the ALLELE FREQUENCY from one generation to the next.Amino Acid Sequence: The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION.Risk Factors: An aspect of personal behavior or lifestyle, environmental exposure, or inborn or inherited characteristic, which, on the basis of epidemiologic evidence, is known to be associated with a health-related condition considered important to prevent.Family Health: The health status of the family as a unit including the impact of the health of one member of the family on the family as a unit and on individual family members; also, the impact of family organization or disorganization on the health status of its members.Pigmentation: Coloration or discoloration of a part by a pigment.Nutrigenomics: The study of the relationship between NUTRITIONAL PHYSIOLOGY and genetic makeup. It includes the effect of different food components on GENE EXPRESSION and how variations in GENES effect responses to food components.Computer Simulation: Computer-based representation of physical systems and phenomena such as chemical processes.History, 19th Century: Time period from 1801 through 1900 of the common era.Genes: A category of nucleic acid sequences that function as units of heredity and which code for the basic instructions for the development, reproduction, and maintenance of organisms.Diseases in Twins: Disorders affecting TWINS, one or both, at any age.Gene Expression Profiling: The determination of the pattern of genes expressed at the level of GENETIC TRANSCRIPTION, under specific circumstances or in a specific cell.Genes, Recessive: Genes that influence the PHENOTYPE only in the homozygous state.Lod Score: The total relative probability, expressed on a logarithmic scale, that a linkage relationship exists among selected loci. Lod is an acronym for "logarithmic odds."Algorithms: A procedure consisting of a sequence of algebraic formulas and/or logical steps to calculate or determine a given task.Mutagenesis: Process of generating a genetic MUTATION. It may occur spontaneously or be induced by MUTAGENS.Twins, Monozygotic: Two off-spring from the same PREGNANCY. They are from a single fertilized OVUM that split into two EMBRYOS. Such twins are usually genetically identical and of the same sex.Genes, Dominant: Genes that influence the PHENOTYPE both in the homozygous and the heterozygous state.Polymerase Chain Reaction: In vitro method for producing large amounts of specific DNA or RNA fragments of defined length and sequence from small amounts of short oligonucleotide flanking sequences (primers). The essential steps include thermal denaturation of the double-stranded target molecules, annealing of the primers to their complementary sequences, and extension of the annealed primers by enzymatic synthesis with DNA polymerase. The reaction is efficient, specific, and extremely sensitive. Uses for the reaction include disease diagnosis, detection of difficult-to-isolate pathogens, mutation analysis, genetic testing, DNA sequencing, and analyzing evolutionary relationships.Mutagenesis, Insertional: Mutagenesis where the mutation is caused by the introduction of foreign DNA sequences into a gene or extragenic sequence. This may occur spontaneously in vivo or be experimentally induced in vivo or in vitro. Proviral DNA insertions into or adjacent to a cellular proto-oncogene can interrupt GENETIC TRANSLATION of the coding sequences or interfere with recognition of regulatory elements and cause unregulated expression of the proto-oncogene resulting in tumor formation.Genes, Insect: The functional hereditary units of INSECTS.Haploidy: The chromosomal constitution of cells, in which each type of CHROMOSOME is represented once. Symbol: N.Internet: A loose confederation of computer communication networks around the world. The networks that make up the Internet are connected through several backbone networks. The Internet grew out of the US Government ARPAnet project and was designed to facilitate information exchange.DNA Mutational Analysis: Biochemical identification of mutational changes in a nucleotide sequence.Population Dynamics: The pattern of any process, or the interrelationship of phenomena, which affects growth or change within a population.Societies, Scientific: Societies whose membership is limited to scientists.Likelihood Functions: Functions constructed from a statistical model and a set of observed data which give the probability of that data for various values of the unknown model parameters. Those parameter values that maximize the probability are the maximum likelihood estimates of the parameters.Systems Biology: Comprehensive, methodical analysis of complex biological systems by monitoring responses to perturbations of biological processes. Large scale, computerized collection and analysis of the data are used to develop and test models of biological systems.Epigenesis, Genetic: A genetic process by which the adult organism is realized via mechanisms that lead to the restriction in the possible fates of cells, eventually leading to their differentiated state. Mechanisms involved cause heritable changes to cells without changes to DNA sequence such as DNA METHYLATION; HISTONE modification; DNA REPLICATION TIMING; NUCLEOSOME positioning; and heterochromatization which result in selective gene expression or repression.Crops, Agricultural: Cultivated plants or agricultural produce such as grain, vegetables, or fruit. (From American Heritage Dictionary, 1982)Genotyping Techniques: Methods used to determine individuals' specific ALLELES or SNPS (single nucleotide polymorphisms).Arabidopsis: A plant genus of the family BRASSICACEAE that contains ARABIDOPSIS PROTEINS and MADS DOMAIN PROTEINS. The species A. thaliana is used for experiments in classical plant genetics as well as molecular genetic studies in plant physiology, biochemistry, and development.Homozygote: An individual in which both alleles at a given locus are identical.Heterozygote Detection: Identification of genetic carriers for a given trait.Zebrafish: An exotic species of the family CYPRINIDAE, originally from Asia, that has been introduced in North America. They are used in embryological studies and to study the effects of certain chemicals on development.Chromosomes, Human: Very long DNA molecules and associated proteins, HISTONES, and non-histone chromosomal proteins (CHROMOSOMAL PROTEINS, NON-HISTONE). Normally 46 chromosomes, including two sex chromosomes are found in the nucleus of human cells. They carry the hereditary information of the individual.Twins, Dizygotic: Two offspring from the same PREGNANCY. They are from two OVA, fertilized at about the same time by two SPERMATOZOA. Such twins are genetically distinct and can be of different sexes.Bayes Theorem: A theorem in probability theory named for Thomas Bayes (1702-1761). In epidemiology, it is used to obtain the probability of disease in a group of people with some characteristic on the basis of the overall rate of that disease and of the likelihood of that characteristic in healthy and diseased individuals. The most familiar application is in clinical decision analysis where it is used for estimating the probability of a particular diagnosis given the appearance of some symptoms or test result.Family: A social group consisting of parents or parent substitutes and children.Flowers: The reproductive organs of plants.Cluster Analysis: A set of statistical methods used to group variables or observations into strongly inter-related subgroups. In epidemiology, it may be used to analyze a closely grouped series of events or cases of disease or other health-related phenomenon with well-defined distribution patterns in relation to time or place or both.Phylogeography: A field of study concerned with the principles and processes governing the geographic distributions of genealogical lineages, especially those within and among closely related species. (Avise, J.C., Phylogeography: The History and Formation of Species. Harvard University Press, 2000)Genetic Complementation Test: A test used to determine whether or not complementation (compensation in the form of dominance) will occur in a cell with a given mutant phenotype when another mutant genome, encoding the same mutant phenotype, is introduced into that cell.Age of Onset: The age, developmental stage, or period of life at which a disease or the initial symptoms or manifestations of a disease appear in an individual.Caenorhabditis elegans: A species of nematode that is widely used in biological, biochemical, and genetic studies.EuropeDisease: A definite pathologic process with a characteristic set of signs and symptoms. It may affect the whole body or any of its parts, and its etiology, pathology, and prognosis may be known or unknown.Neoplasms: New abnormal growth of tissue. Malignant neoplasms show a greater degree of anaplasia and have the properties of invasion and metastasis, compared to benign neoplasms.Ecology: The branch of science concerned with the interrelationship of organisms and their ENVIRONMENT, especially as manifested by natural cycles and rhythms, community development and structure, interactions between different kinds of organisms, geographic distributions, and population alterations. (Webster's, 3d ed)Neoplastic Syndromes, Hereditary: The condition of a pattern of malignancies within a family, but not every individual's necessarily having the same neoplasm. Characteristically the tumor tends to occur at an earlier than average age, individuals may have more than one primary tumor, the tumors may be multicentric, usually more than 25 percent of the individuals in direct lineal descent from the proband are affected, and the cancer predisposition in these families behaves as an autosomal dominant trait with about 60 percent penetrance.Genetic Enhancement: The use of genetic methodologies to improve functional capacities of an organism rather than to treat disease.Penetrance: The percent frequency with which a dominant or homozygous recessive gene or gene combination manifests itself in the phenotype of the carriers. (From Glossary of Genetics, 5th ed)Diploidy: The chromosomal constitution of cells, in which each type of CHROMOSOME is represented twice. Symbol: 2N or 2X.Curriculum: A course of study offered by an educational institution.United StatesSchizophrenia: A severe emotional disorder of psychotic depth characteristically marked by a retreat from reality with delusion formation, HALLUCINATIONS, emotional disharmony, and regressive behavior.Oligonucleotide Array Sequence Analysis: Hybridization of a nucleic acid sample to a very large set of OLIGONUCLEOTIDE PROBES, which have been attached individually in columns and rows to a solid support, to determine a BASE SEQUENCE, or to detect variations in a gene sequence, GENE EXPRESSION, or for GENE MAPPING.Sequence Alignment: The arrangement of two or more amino acid or base sequences from an organism or organisms in such a way as to align areas of the sequences sharing common properties. The degree of relatedness or homology between the sequences is predicted computationally or statistically based on weights assigned to the elements aligned between the sequences. This in turn can serve as a potential indicator of the genetic relatedness between the organisms.Mice, Inbred Strains: Genetically identical individuals developed from brother and sister matings which have been carried out for twenty or more generations, or by parent x offspring matings carried out with certain restrictions. All animals within an inbred strain trace back to a common ancestor in the twentieth generation.Cloning, Molecular: The insertion of recombinant DNA molecules from prokaryotic and/or eukaryotic sources into a replicating vehicle, such as a plasmid or virus vector, and the introduction of the resultant hybrid molecules into recipient cells without altering the viability of those cells.Syndrome: A characteristic symptom complex.Endangered Species: An animal or plant species in danger of extinction. Causes can include human activity, changing climate, or change in predator/prey ratios.High-Throughput Nucleotide Sequencing: Techniques of nucleotide sequence analysis that increase the range, complexity, sensitivity, and accuracy of results by greatly increasing the scale of operations and thus the number of nucleotides, and the number of copies of each nucleotide sequenced. The sequencing may be done by analysis of the synthesis or ligation products, hybridization to preexisting sequences, etc.Virulence: The degree of pathogenicity within a group or species of microorganisms or viruses as indicated by case fatality rates and/or the ability of the organism to invade the tissues of the host. The pathogenic capacity of an organism is determined by its VIRULENCE FACTORS.Chromosomes: In a prokaryotic cell or in the nucleus of a eukaryotic cell, a structure consisting of or containing DNA which carries the genetic information essential to the cell. (From Singleton & Sainsbury, Dictionary of Microbiology and Molecular Biology, 2d ed)Genome, Mitochondrial: The genetic complement of MITOCHONDRIA as represented in their DNA.DNA Primers: Short sequences (generally about 10 base pairs) of DNA that are complementary to sequences of messenger RNA and allow reverse transcriptases to start copying the adjacent sequences of mRNA. Primers are used extensively in genetic and molecular biology techniques.Alcoholism: A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)Multigene Family: A set of genes descended by duplication and variation from some ancestral gene. Such genes may be clustered together on the same chromosome or dispersed on different chromosomes. Examples of multigene families include those that encode the hemoglobins, immunoglobulins, histocompatibility antigens, actins, tubulins, keratins, collagens, heat shock proteins, salivary glue proteins, chorion proteins, cuticle proteins, yolk proteins, and phaseolins, as well as histones, ribosomal RNA, and transfer RNA genes. The latter three are examples of reiterated genes, where hundreds of identical genes are present in a tandem array. (King & Stanfield, A Dictionary of Genetics, 4th ed)Models, Statistical: Statistical formulations or analyses which, when applied to data and found to fit the data, are then used to verify the assumptions and parameters used in the analysis. Examples of statistical models are the linear model, binomial model, polynomial model, two-parameter model, etc.Expressed Sequence Tags: Partial cDNA (DNA, COMPLEMENTARY) sequences that are unique to the cDNAs from which they were derived.Plants: Multicellular, eukaryotic life forms of kingdom Plantae (sensu lato), comprising the VIRIDIPLANTAE; RHODOPHYTA; and GLAUCOPHYTA; all of which acquired chloroplasts by direct endosymbiosis of CYANOBACTERIA. They are characterized by a mainly photosynthetic mode of nutrition; essentially unlimited growth at localized regions of cell divisions (MERISTEMS); cellulose within cells providing rigidity; the absence of organs of locomotion; absence of nervous and sensory systems; and an alternation of haploid and diploid generations.European Continental Ancestry Group: Individuals whose ancestral origins are in the continent of Europe.MedlinePlus: NATIONAL LIBRARY OF MEDICINE service for health professionals and consumers. It links extensive information from the National Institutes of Health and other reviewed sources of information on specific diseases and conditions.Zoology: The study of animals - their morphology, growth, distribution, classification, and behavior.Prenatal Diagnosis: Determination of the nature of a pathological condition or disease in the postimplantation EMBRYO; FETUS; or pregnant female before birth.Principal Component Analysis: Mathematical procedure that transforms a number of possibly correlated variables into a smaller number of uncorrelated variables called principal components.Cell Line: Established cell cultures that have the potential to propagate indefinitely.Neurobiology: The study of the structure, growth, activities, and functions of NEURONS and the NERVOUS SYSTEM.DNA Transposable Elements: Discrete segments of DNA which can excise and reintegrate to another site in the genome. Most are inactive, i.e., have not been found to exist outside the integrated state. DNA transposable elements include bacterial IS (insertion sequence) elements, Tn elements, the maize controlling elements Ac and Ds, Drosophila P, gypsy, and pogo elements, the human Tigger elements and the Tc and mariner elements which are found throughout the animal kingdom.Amplified Fragment Length Polymorphism Analysis: The detection of RESTRICTION FRAGMENT LENGTH POLYMORPHISMS by selective PCR amplification of restriction fragments derived from genomic DNA followed by electrophoretic analysis of the amplified restriction fragments.Adaptation, Biological: Changes in biological features that help an organism cope with its ENVIRONMENT. These changes include physiological (ADAPTATION, PHYSIOLOGICAL), phenotypic and genetic changes.Twins: Two individuals derived from two FETUSES that were fertilized at or about the same time, developed in the UTERUS simultaneously, and born to the same mother. Twins are either monozygotic (TWINS, MONOZYGOTIC) or dizygotic (TWINS, DIZYGOTIC).Gene Expression Regulation: Any of the processes by which nuclear, cytoplasmic, or intercellular factors influence the differential control (induction or repression) of gene action at the level of transcription or translation.Ecosystem: A functional system which includes the organisms of a natural community together with their environment. (McGraw Hill Dictionary of Scientific and Technical Terms, 4th ed)Animals, Genetically Modified: ANIMALS whose GENOME has been altered by GENETIC ENGINEERING, or their offspring.Gene Regulatory Networks: Interacting DNA-encoded regulatory subsystems in the GENOME that coordinate input from activator and repressor TRANSCRIPTION FACTORS during development, cell differentiation, or in response to environmental cues. The networks function to ultimately specify expression of particular sets of GENES for specific conditions, times, or locations.Signal Transduction: The intracellular transfer of information (biological activation/inhibition) through a signal pathway. In each signal transduction system, an activation/inhibition signal from a biologically active molecule (hormone, neurotransmitter) is mediated via the coupling of a receptor/enzyme to a second messenger system or to an ion channel. Signal transduction plays an important role in activating cellular functions, cell differentiation, and cell proliferation. Examples of signal transduction systems are the GAMMA-AMINOBUTYRIC ACID-postsynaptic receptor-calcium ion channel system, the receptor-mediated T-cell activation pathway, and the receptor-mediated activation of phospholipases. Those coupled to membrane depolarization or intracellular release of calcium include the receptor-mediated activation of cytotoxic functions in granulocytes and the synaptic potentiation of protein kinase activation. Some signal transduction pathways may be part of larger signal transduction pathways; for example, protein kinase activation is part of the platelet activation signal pathway.Virus Replication: The process of intracellular viral multiplication, consisting of the synthesis of PROTEINS; NUCLEIC ACIDS; and sometimes LIPIDS, and their assembly into a new infectious particle.Ethics, Medical: The principles of professional conduct concerning the rights and duties of the physician, relations with patients and fellow practitioners, as well as actions of the physician in patient care and interpersonal relations with patient families.Influenza A virus: The type species of the genus INFLUENZAVIRUS A that causes influenza and other diseases in humans and animals. Antigenic variation occurs frequently between strains, allowing classification into subtypes and variants. Transmission is usually by aerosol (human and most non-aquatic hosts) or waterborne (ducks). Infected birds shed the virus in their saliva, nasal secretions, and feces.Population Density: Number of individuals in a population relative to space.Chromosome Aberrations: Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS.DNA: A deoxyribonucleotide polymer that is the primary genetic material of all cells. Eukaryotic and prokaryotic organisms normally contain DNA in a double-stranded state, yet several important biological processes transiently involve single-stranded regions. DNA, which consists of a polysugar-phosphate backbone possessing projections of purines (adenine and guanine) and pyrimidines (thymine and cytosine), forms a double helix that is held together by hydrogen bonds between these purines and pyrimidines (adenine to thymine and guanine to cytosine).Reproduction, Asexual: Reproduction without fusion of two types of cells, mostly found in ALGAE; FUNGI; and PLANTS. Asexual reproduction occurs in several ways, such as budding, fission, or splitting from "parent" cells. Only few groups of ANIMALS reproduce asexually or unisexually (PARTHENOGENESIS).Hair Color: Color of hair or fur.DNA, Helminth: Deoxyribonucleic acid that makes up the genetic material of helminths.History, Ancient: The period of history before 500 of the common era.Genome, Viral: The complete genetic complement contained in a DNA or RNA molecule in a virus.Gene Deletion: A genetic rearrangement through loss of segments of DNA or RNA, bringing sequences which are normally separated into close proximity. This deletion may be detected using cytogenetic techniques and can also be inferred from the phenotype, indicating a deletion at one specific locus.Longevity: The normal length of time of an organism's life.X Chromosome: The female sex chromosome, being the differential sex chromosome carried by half the male gametes and all female gametes in human and other male-heterogametic species.Bioethics: A branch of applied ethics that studies the value implications of practices and developments in life sciences, medicine, and health care.Biomedical Research: Research that involves the application of the natural sciences, especially biology and physiology, to medicine.Ethylnitrosourea: A nitrosourea compound with alkylating, carcinogenic, and mutagenic properties.Genome, Insect: The genetic complement of an insect (INSECTS) as represented in its DNA.Models, Animal: Non-human animals, selected because of specific characteristics, for use in experimental research, teaching, or testing.Consanguinity: The magnitude of INBREEDING in humans.Genome, Helminth: The genetic complement of a helminth (HELMINTHS) as represented in its DNA.Nursing Education Research: Investigations into the problems of integrating research findings into nursing curricula, developing problem solving skills, finding approaches to clinical teaching, determining the level of practice by graduates from different basic preparations, etc.Molecular Sequence Annotation: The addition of descriptive information about the function or structure of a molecular sequence to its MOLECULAR SEQUENCE DATA record.Plasmids: Extrachromosomal, usually CIRCULAR DNA molecules that are self-replicating and transferable from one organism to another. They are found in a variety of bacterial, archaeal, fungal, algal, and plant species. They are used in GENETIC ENGINEERING as CLONING VECTORS.Ethyl Methanesulfonate: An antineoplastic agent with alkylating properties. It also acts as a mutagen by damaging DNA and is used experimentally for that effect.Gene Expression: The phenotypic manifestation of a gene or genes by the processes of GENETIC TRANSCRIPTION and GENETIC TRANSLATION.User-Computer Interface: The portion of an interactive computer program that issues messages to and receives commands from a user.Gene Expression Regulation, Plant: Any of the processes by which nuclear, cytoplasmic, or intercellular factors influence the differential control of gene action in plants.Reassortant Viruses: Viruses containing two or more pieces of nucleic acid (segmented genome) from different parents. Such viruses are produced in cells coinfected with different strains of a given virus.

*  Home,Population and Disease Genetics Group
Home,Population and Disease Genetics Group. Skip to ... Sclerosis. Population Genetics. Collaborators. Contacts. ... Launch of new genetics and health study in Shetland. I m a ... home population and disease genetics group skip to accessibility options skip to content the university of edinburgh home news team orcades multiple sclerosis population genetics collaborators contacts publications media gallery latest news viking health study shetland dna study shows prince william has indian heritage launch of new genetics and health study in shetland i m a reader in the usher institute for population health sciences and informatics at the university of edinburgh where my group studies population history and structure and the genetics of complex disease i lead the orkney complex disease study orcades and the viking health study shetland both isolated population resources with rich phenotyping deep genotyping tissue biobanks and prospective follow up the studies have contributed to the discovery of over...
http://orcades.ed.ac.uk/
*  .. We provide custom therapies for the prevention, healing and management of chronic and debilitati
10% of the U.S. Population = 35 million people n. May 24th, 2015 ... herbalistandherbs. We provide custom therapies for the prevention, healing and management of chronic and debilitating disorders. How We Help. We apply non-toxic modalities to elicit healing by supporting the body’s self- correcting nature. Learn More. Working Together. Arrange an onsite or online consultation where we develop a natural protocol to bring your health into balance. Learn More. Educate Yourself. Knowledge is key to health and healing. Our blog provides a wealth of information on the key disorders and diseases we work with. Learn More. Connect Book. Connect with Harry directly to learn more or schedule a consultation. Learn More. Latest From The Herbalist and Herbs Blog. DONNIE YANCE: A MISSING KEY IN “A UNIFIED THEORY OF HEALTH AND DISEASE” by Harry Chrissakis, Herbalist. HERBALIST AND HERBS. When I began studying Natural Medicine, some of the minds that influenced me where the German nature healers from around the turn. NEURO...
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*  ExPASy: SIB Bioinformatics Resource Portal - Home
Cell. Organism. Population. Categories. proteomics. protein ... /evolution. population genetics. transcriptomics. biophysics ... , systems biology, population genetics, transcriptomics etc. see ... ExPASy: SIB Bioinformatics Resource Portal - Home. Background and reference. Overview. Disclaimer. Contact. Support. SIB Groups. Find resources Query all databases - Query within a category: genomics phylogeny/evolution proteomics systems biology - Query a specific database: Cellosaurus ENZYME EPD GPSDB HAMAP miROrtho MyHits OMA OpenFlu OrthoDB PROSITE Protein Spotlight Selectome STRING SWISS-2DPAGE SWISS-MODEL Repository SwissDock SwissLipids SwissVar UniProtKB VenomZone ViralZone World-2DPAGE Repository. search help. Protein. Population. Categories. proteomics. protein sequences and identification mass spectrometry and 2-DE data protein characterisation and function families, patterns and profiles post-translational modification protein structure protein-protein interaction similarity search/alignment ...
http://expasy.org/?tab=blast
*  GPS in your DNA: Genetics can reveal your geographic ancestral origin - ScienceBlog.com
GPS in your DNA: Genetics can reveal your geographic ancestral ... GPS in your DNA: Genetics can reveal your geographic ancestral ... the journal Nature Genetics , this method has the potential to...
http://scienceblog.com/56124/gps-in-your-dna-genetics-can-reveal-your-geographic-ancestral-origin/
*  Population genetics
Population genetics. Toggle navigation. Sign Up. Sign In. ... In. Share:. Get Population genetics from Amazon.com. Population genetics Summary. Everything you need to ... Read more. Population Genetics and the Problem of Diversity. ... Read more. Population Genetics. 349 words, approx. 2 pages. Population Genetics Population genetics is the ... Read more. Population Genetics. 794 words, approx. 3 pages. Population Genetics Population genetics is the ... Read more. Population Genetics. 604 words, approx. 3 pages. Population Genetics In the decade between 1858...
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*  NJDEP Division of Fish & Wildlife - 2005 Delaware Shorebird Project Participants
, working on their genetics, population biology and demography....
http://nj.gov/dep/fgw/ensp/delbayteam05.htm
*  .. Why Doesn’t Everyone Get Alzheimer’s?
through DeCODE Genetics, a company which scanned the entire DNA ... Icelanders. This population is a relatively homogeneous group, with ... They found a mutation in a particular gene significantly over-represented in this group, suggesting that this mutation might be involved in protection from Alzheimer’s. This report suggests that there are genetic mutations which protect against Alzheimer’s disease, and that in this case they work by diminishing the production of amyloid beta. Thus if you could either slow down the production of Abeta42 or remove it from the brain there would be a treatment for the disease. Most of the people with Alzheimer’s disease may have a family history, but no specifically identified genetic abnormality. But a small population about 1 percent has a dominantly inherited form. In this situation, if you have mutations in one of three identified genes, you will get the disease. An international consortium to study these dominantly inherited subjects, known as the Dominantly Inhe...
http://dementiatoday.com/why-doesnt-everyone-get-alzheimers/
*  Advanced Microscopy Core (JDC) | Core Facilities | Harvard Catalyst
IND/IDE studies. Population Health Research Consulting Training and ... the T spectrum. Genetics Bioinformatics Courses Courses on ... in translational genetics bioinformatics. Health Disparities ... Advanced Microscopy Core JDC. Core Facilities. Imaging Facilitation Connecting investigators with medical imaging experts. Genetics Bioinformatics Courses Courses on general and specialized topics in translational genetics bioinformatics. Biostatistics Training A 60-credit HSPH master of science program in applied biostatistics. Core Facilities A searchable database of core laboratory facilities. HCCRC Lab Services Laboratory assay consulting, new assay development, and subsidized research tests. HCCRC Protocol Review Access the resources of five Harvard- and MIT-affiliated clinical research centers. Harvard Catalyst Clinical Research Center HCCRC Access the resources of five Harvard Catalyst clinical research centers. Beth Israel Deaconess Medical Center BIDMC BADERC Metabolic Physiology Core HMS. Dana-Fa...
http://cbmi.catalyst.harvard.edu/cores/ins/core.html?core_id=129&uri_id=0000012e-587f-da55-55da-381e80000000&institution_id=20&navMode=ins
*  FORCE | Finding Specialists & Paying for Care : Privacy & Legal Issues
Hereditary Cancer & Genetics. Genetic Counseling & Risk Assessment ... Tool. Special Populations Cancer Previvors. Breast Cancer ... FORCE. Finding Specialists & Paying for Care : Privacy & Legal Issues. Understanding BRCA & HBOC. Our Role & Impact. Hereditary Cancer Hereditary Cancer & Genetics. Genetic Counseling & Risk Assessment. BRCA Mutations and Cancer. Genes Associated with Known Hereditary Cancer Syndromes. Other Genes Associated with Increased Breast and/or Ovarian Cancer Risk. Cancer Risk Breast Cancer. Ovarian & Related Cancer. Other Cancers. Risk Management Risk Management Guidelines. Breast Cancer Screening. Breast Cancer Chemoprevention. Mastectomy. Ovarian Cancer Screening. Ovarian Cancer Chemoprevention. Screening and Prevention of Other Cancers. Surgeon Referral Tool. Breast Reconstruction Reconstruction Overview. Types of Reconstruction. Surgeon Referral Tool. Post Mastectomy and Reconstruction Photos. Cancer Treatment BRCA & Treatment Options. Breast Cancer Treatment. Ovarian Cancer T...
http://facingourrisk.org/understanding-brca-and-hboc/information/finding-health-care/insurance-privacy-issues/index.php
*  Asia Cohort Consortium
between genetics, environmental exposures, and the ... between genetics, environmental exposures, and the ... of a cohort, or population laboratory, of at least 1 million ... Asia Cohort Consortium. Public Health Sciences Labs Projects Asia Cohort Consortium. Asia Cohort Consortium. Rationale Overview ACC Portal The Asia Cohort Consortium ACC is a collaborative effort seeking to understand the relationship between genetics, environmental exposures, and the etiology of disease through the establishment of a cohort of at least one million healthy people around the world. We also thank the Fred Hutch for its continued support of the Coordinating Center. Coordinating Centers in Cancer-Epidemiology Research: The Asia Cohort Consortium Coordinating Center Cancer Epidemiology, Biomarkers and Prevention. Rationale The Asia Cohort Consortium ACC seeks to understand the relationship between genetics, environmental exposures, and the etiology of disease through the establishment of a cohort, or population laborator...
https://fredhutch.org/en/labs/phs/projects/asia-cohort-consortium.html
*  Walter Reed Army Institute of Research
... Image: The "Daniel Inouye Building" Building 503, Forest Glen Annex, Silver Spring, Maryland — home to the 'WRAIR' since 1999. The 'Walter Reed Army Institute of Research' 'WRAIR' is the largest biomedical research facility administered by the U.S. The institute is centered at the Forest Glen Annex, part of the unincorporated Silver Spring urban area in Maryland just north of Washington, DC, but it is a subordinate unit of the U.S. Inouye Building, also known as Building 503 — with the Naval Medical Research Center since 1999. Divisions and Subordinate Units of the WRAIR Divisions at the Daniel K. The Walter Reed Army Institute of Research hosts two Centers of Excellence for Military Psychiatry and Neuroscience and for Infectious Disease Research which are headquartered in Silver Spring, Maryland. Bacterial Diseases Entomology Program United States Military HIV Research Program Makerere University Walter Reed Project MUWRP. Military Malaria Research Program Preventive Medicine Program Viral Diseases. Sci...
https://en.wikipedia.org/wiki/Walter_Reed_Army_Institute_of_Research
*  Nancy J Wesensten
2002 Performance and alertness effects of caffeine, dextroamphetamine, and modafinil during sleep deprivation Nancy J Wesensten Division of Psychiatry and Neuroscience, Department of Behavioral Biology, Walter Reed Army Institute of Research, Silver Spring, MD 20910, USA J Sleep Res 14:255-66. 2005 Effects of modafinil on cognitive performance and alertness during sleep deprivation Nancy J Wesensten Department of Behavioral Biology, Division of Psychiatry and Neuroscience, Walter Reed Army Institute of Research, 503 Robert Grant Avenue, Silver Spring, MD 20910 7500, USA Curr Pharm Des 12:2457-71. Performance and alertness effects of caffeine, dextroamphetamine, and modafinil during sleep deprivation Nancy J Wesensten Division of Psychiatry and Neuroscience, Department of Behavioral Biology, Walter Reed Army Institute of Research, Silver Spring, MD 20910, USA J Sleep Res 14:255-66. Effects of modafinil on cognitive performance and alertness during sleep deprivation Nancy J Wesensten Department of Behavioral Bi...
http://labome.org/expert/usa/walter/wesensten/nancy-j-wesensten-236300.html
*  N L Michael
2009 Development of calibrated viral load standards for group M subtypes of human immunodeficiency virus type 1 and performance of an improved AMPLICOR HIV-1 MONITOR test with isolates of diverse subtypes N L Michael Division of Retrovirology, Walter Reed Army Institute of Research, Rockville, Maryland 20850, USA J Clin Microbiol 37:2557-63. 2001 Use of calibrated viral load standards for group M subtypes of human immunodeficiency virus type 1 to assess the performance of viral RNA quantitation tests L L Jagodzinski Henry M Jackson Foundation, Walter Reed Army Institute of Research, Rockville, Maryland 20850, USA J Clin Microbiol 38:1247-9. 2001 High-throughput genotyping of KIR2DL2/L3, KIR3DL1/S1, and their HLA class I ligands using real-time PCR R N Koehler Division of Retrovirology, US Military HIV Research Program Henry M Jackson Foundation, Rockville, MD 20850, USA Tissue Antigens 74:73-80. Development of calibrated viral load standards for group M subtypes of human immunodeficiency virus type 1 and perf...
http://labome.org/expert/michael/n-l-michael-683817.html
*  Gregor Mendel Institute
... The 'Gregor Mendel Institute of Molecular Plant Biology' 'GMI' was founded by the Austrian Academy of Sciences in 2000 to promote research excellence in the area of molecular plant biology. Research at the GMI is curiosity driven and covers many aspects of molecular genetics, including basic mechanisms of epigenetics, population genetics, chromosome biology, developmental biology, stress signal transduction and plant pathogens. The institute is named after Gregor Mendel, the ‘father of genetics ’, who studied at the University of Vienna in the middle of the 19th century. The Gregor Mendel Institute was founded on the initiative of the Presidency of the Austrian Academy of Sciences and Dr Dieter Schweizer. The location was planned for the Vienna Biocenter, with a focus on basic research in molecular plant biology, as complement to the research of the neighboring campus institutes and the biomedical, also of the Austrian Academy of Sciences. In 2004, the GMI welcomed two new research groups: Dr Marjori Mat...
https://en.wikipedia.org/wiki/Gregor_Mendel_Institute
*  Gregor Samsa Latest Albums | MTV
gregor samsa latest albums mtv get the mtv artists app and discover music wherever you are gregor samsa discography discography from position showing items asking see all now playing gregor samsa over air kora records now playing gregor samsa rest the kora records now playing gregor samsa own music now playing gregor samsa iodine are you gregor samsa claim this page learn more about mtv artists faq for artists gregor samsa bio gregor samsa tour dates gregor samsa music gregor samsa video news gregor samsa photos gregor samsa news gregor samsa discography mtv mtv jobs terms of use privacy policy user content agreement copyright compliance policy artist index ad choices this site contains content from artists fans and writers from around the internet in it s natural form such content is not representative of viacom media networks viacom international inc all rights reserved mtv and all related titles and logos are trademarks of viacom international inc beta explore artists popular collections artist to watch yo...
http://mtv.com/artists/gregor-samsa/discography/
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Gaucher Disease tests available. Glucocerebrosidase Deficiency. Glucosylceramidase Deficiency. Gaucher Disease Type 1. Gaucher Disease Type 2 Acute. Gaucher Disease Type 3 Subacute/Chronic. Gaucher Disease Cardiovascular Form. Gaucher Disease Perinatal-Lethal Form Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Enzyme Analysis Beta-Glucosidase Enzyme Analysis Test Code: 4554. Mutation Analysis Gaucher Disease Ashkenazic Mutation Panel Test Code: 6033. Gauc...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Add to Custom Req. Print Req Chromosome Analysis - Blood chromosomes. chromosome analysis. Test Information: Confirmation of clinical diagnosis. Test Details Test Code: 8600. Technical Information Methodology: Standard methodology is used for G-banded chromosome Analysis. Sample & Shipping Information Test Requisition: Cytogenetics. Specimen Type: Blood. Requirements: Draw blood in a green-top Sodium Heparin tube s and send 3-5 mL adults/child or 1-2 ml < 3 months. Shipping Conditions: Ship the sample at room temperature to the laboratory by overnight express. Specimen should arrive in the laboratory within 48 hrs of sample date. Specimen can...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Methylcobalamin Deficiency, cblG Type MTR tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis MTR Deletion/Duplication Analysis Test Code: 2053. Sequence & Deletion/Duplication Analysis MTR Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2054. Sequence Analysis MTR Sequence Analysis Test Code: 2050. MTR Sequence Analysis Test Code: 2051 This test can only be performed if there is a previously identified familial mutation. MTR Sequence...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. MRPS2 Related disorders tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis MRPS2 Deletion/Duplication Analysis Test Code: 2283. Sequence & Deletion/Duplication Analysis MRPS2 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2284. Sequence Analysis MRPS2 Sequence Analysis Test Code: 2280. MRPS2 Sequence Analysis Test Code: 2281 This test can only be performed if there is a previously identified familial mutation. MRPS2 Sequence Analysi...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. B4GALT7 Related Disorders tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis B4GALT7 Deletion/Duplication Analysis Test Code: 3298. Sequence & Deletion/Duplication Analysis B4GALT7 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3299. Sequence Analysis B4GALT7 Sequence Analysis Test Code: 3295. B4GALT7 Sequence Analysis Test Code: 3296 This test can only be performed if there is a previously identified familial mutation. B4GALT7 Sequ...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. B4GALT7 Related Disorders tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis B4GALT7 Deletion/Duplication Analysis Test Code: 3298. Sequence & Deletion/Duplication Analysis B4GALT7 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3299. Sequence Analysis B4GALT7 Sequence Analysis Test Code: 3295. B4GALT7 Sequence Analysis Test Code: 3296 This test can only be performed if there is a previously identified familial mutation. B4GALT7 Sequ...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. 2,4-Dienoyl-CoA Reductase Deficiency DECR1 tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis DECR1 Deletion/Duplication Analysis Test Code: 5038. Sequence & Deletion/Duplication Analysis DECR1 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 5039. Sequence Analysis DECR1 Sequence Analysis Test Code: 5035. DECR1 Sequence Analysis Test Code: 5036 This test can only be performed if there is a previously identified familial mutation. DEC...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Von Hippel Lindau Syndrome tests available. VHL Syndrome. von Hippel-Lindau Disease. Von Hippel-Lindau Syndrome Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis VHL Deletion/Duplication Analysis Test Code: 6775. VHL Deletion/Duplication Analysis Test Code: 6775. VHL Deletion/Duplication Analysis Test Code: 6776 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submitting any samples. VHL Deletion/Duplication Analysis Test Code: 6775. Sequence & Deletion/Duplication Analysis VHL Comprehensive - ...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. RP2-Related Retinitis Pigmentosa tests available. Retinitis Pigmentosa 2 Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis RP2 Deletion/Duplication Analysis Test Code: 2448. Sequence & Deletion/Duplication Analysis RP2 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2449. Sequence Analysis RP2 Sequence Analysis Test Code: 2445. RP2 Sequence Analysis Test Code: 2446 This test can only be performed if there is a previously identified familial mutation...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Osteopathia Striata with Cranial Sclerosis tests available. AMER1. FAM123B Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis AMER1 Deletion/Duplication Analysis Test Code: 2573. Sequence & Deletion/Duplication Analysis AMER1 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2574. Sequence Analysis AMER1 Sequence Analysis Test Code: 2570. AMER1 Sequence Analysis Test Code: 2571 This test can only be performed if there is a previously identified familia...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Osteopetrosis with Renal Tubular Acidosis CA2 tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis CA2 Deletion/Duplication Analysis Test Code: 2603. Sequence & Deletion/Duplication Analysis CA2 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2604. Sequence Analysis CA2 Sequence Analysis Test Code: 2600. CA2 Sequence Analysis Test Code: 2601 This test can only be performed if there is a previously identified familial mutation. CA2 Sequ...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. SP7-Related Osteogenesis Imperfecta tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis SP7 Deletion/Duplication Analysis Test Code: 2698. Sequence & Deletion/Duplication Analysis SP7 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2699. Sequence Analysis SP7 Sequence Analysis Test Code: 2695. SP7 Sequence Analysis Test Code: 2696 This test can only be performed if there is a previously identified familial mutation. SP7 Sequence Analy...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Mitochondrial Complex IV Deficiency-COX4I1 Related tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis COX4I1 Deletion/Duplication Analysis Test Code: 2733. Sequence & Deletion/Duplication Analysis COX4I1 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2734. Sequence Analysis COX4I1 Sequence Analysis Test Code: 2730. COX4I1 Sequence Analysis Test Code: 2731 This test can only be performed if there is a previously identified familial m...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2730
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Mitochondrial Complex V Deficiency-ATPAF2 Related ATP12 tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis ATPAF2 Deletion/Duplication Analysis Test Code: 3273. Sequence & Deletion/Duplication Analysis ATPAF2 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3274. Sequence Analysis ATPAF2 Sequence Analysis Test Code: 3270. ATPAF2 Sequence Analysis Test Code: 3271 This test can only be performed if there is a previously identified famil...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3270
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis ROM1 Deletion/Duplication Analysis Test Code: 2813. Sequence & Deletion/Duplication Analysis ROM1 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2814. Sequence Analysis ROM1 Sequence Analysis Test Code: 2810. ROM1 Sequence Analysis Test Code: 2811 This test can only be performed if there is a previously identified familial mutation. ROM1 Sequence Analysis Test Code: 2812 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submi...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2814&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis PPIB Deletion/Duplication Analysis Test Code: 2618. Sequence & Deletion/Duplication Analysis PPIB Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2619. Sequence Analysis PPIB Sequence Analysis Test Code: 2615. PPIB Sequence Analysis Test Code: 2616 This test can only be performed if there is a previously identified familial mutation. PPIB Sequence Analysis Test Code: 2617 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submi...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2619&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis MCEE Deletion/Duplication Analysis Test Code: 3398. Sequence & Deletion/Duplication Analysis MCEE Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3399. Sequence Analysis MCEE Sequence Analysis Test Code: 3395. MCEE Sequence Analysis Test Code: 3396 This test can only be performed if there is a previously identified familial mutation. MCEE Sequence Analysis Test Code: 3397 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submi...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3399&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis NDUFS6 Deletion/Duplication Analysis Test Code: 3568. Sequence & Deletion/Duplication Analysis NDUFS6 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3569. Sequence Analysis NDUFS6 Sequence Analysis Test Code: 3565. NDUFS6 Sequence Analysis Test Code: 3566 This test can only be performed if there is a previously identified familial mutation. NDUFS6 Sequence Analysis Test Code: 3567 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submitting any samples. Print Req ND...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3569&show=1&cfid=340488137&cftoken=46268151
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis TCN2 Deletion/Duplication Analysis Test Code: 3968. Sequence & Deletion/Duplication Analysis TCN2 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3969. Sequence Analysis TCN2 Sequence Analysis Test Code: 3965. TCN2 Sequence Analysis Test Code: 3966 This test can only be performed if there is a previously identified familial mutation. TCN2 Sequence Analysis Test Code: 3967 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submi...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3969&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. MRPS18A Related Disorders tests available. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis MRPS18A Deletion/Duplication Analysis Test Code: 2298. Sequence & Deletion/Duplication Analysis MRPS18A Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2299. Sequence Analysis MRPS18A Sequence Analysis Test Code: 2295. MRPS18A Sequence Analysis Test Code: 2296 This test can only be performed if there is a previously identified familial mutation. MRPS18A Sequence Analysis Test Code: 2297 We require that the referring center consult with our laboratory ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2299&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. FAM20C Related Disorders tests available. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis FAM20C Deletion/Duplication Analysis Test Code: 2578. Sequence & Deletion/Duplication Analysis FAM20C Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2579. Sequence Analysis FAM20C Sequence Analysis Test Code: 2575. FAM20C Sequence Analysis Test Code: 2576 This test can only be performed if there is a previously identified familial mutation. FAM20C Sequence Analysis Test Code: 2577 We require that the referring center consult with our laboratory geneti...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2579&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis SNRNP200 Deletion/Duplication Analysis Test Code: 2818. Sequence & Deletion/Duplication Analysis SNRNP200 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2819. Sequence Analysis SNRNP200 Sequence Analysis Test Code: 2815. SNRNP200 Sequence Analysis Test Code: 2816 This test can only be performed if there is a previously identified familial mutation. SNRNP200 Sequence Analysis Test Code: 2817 We require that the referring center consult with our laboratory genetic counselors regarding prenatal ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2819&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis GALT Deletion/Duplication Analysis Test Code: 3248. Sequence & Deletion/Duplication Analysis GALT Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3249. Sequence Analysis GALT Sequence Analysis Test Code: 3245. GALT Sequence Analysis Test Code: 3246 This test can only be performed if there is a previously identified familial mutation. GALT Prenatal Sequence Analysis GeneAware Test Code: 60377 We require that the referring center consult with our laboratory genetic counselors regarding prenatal ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3249&show=1&cfid=340532288&cftoken=25369977
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis ACAT1 Deletion/Duplication Analysis Test Code: 2268. Sequence & Deletion/Duplication Analysis ACAT1 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2269. Sequence Analysis ACAT1 Sequence Analysis Test Code: 2265. ACAT1 Sequence Analysis Test Code: 2266 This test can only be performed if there is a previously identified familial mutation. ACAT1 Sequence Analysis Test Code: 2267 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2269&show=1&cfid=340487628&cftoken=15990732
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Glycogen Storage Disease Type 0, Liver Isoform tests available. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis GYS2 Deletion/Duplication Analysis Test Code: 3533. Sequence & Deletion/Duplication Analysis GYS2 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3534. Sequence Analysis GYS2 Sequence Analysis Test Code: 3530. GYS2 Sequence Analysis Test Code: 3531 This test can only be performed if there is a previously identified familial mutation. GYS2 Sequence Analysis Test Code: 3532 We require that the referring center consult with our labor...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3534&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis PUS1 Deletion/Duplication Analysis Test Code: 3653. Sequence & Deletion/Duplication Analysis PUS1 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3654. Sequence Analysis PUS1 Sequence Analysis Test Code: 3650. PUS1 Sequence Analysis Test Code: 3651 This test can only be performed if there is a previously identified familial mutation. PUS1 Sequence Analysis Test Code: 3652 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submi...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3654&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis ALDH4A1 Deletion/Duplication Analysis Test Code: 5138. Sequence & Deletion/Duplication Analysis ALDH4A1 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 5139. Sequence Analysis ALDH4A1 Sequence Analysis Test Code: 5135. ALDH4A1 Sequence Analysis Test Code: 5136 This test can only be performed if there is a previously identified familial mutation. ALDH4A1 Sequence Analysis Test Code: 5137 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=5139&show=1&cfid=329932267&cftoken=74842750
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Mitochondrial Complex I Deficiency-NDUFB6 Related tests available. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis NDUFB6 Deletion/Duplication Analysis Test Code: 2503. Sequence & Deletion/Duplication Analysis NDUFB6 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2504. Sequence Analysis NDUFB6 Sequence Analysis Test Code: 2500. NDUFB6 Sequence Analysis Test Code: 2501 This test can only be performed if there is a previously identified familial mutation. NDUFB6 Sequence Analysis Test Code: 2502 We require that the referring center consult with our laboratory genetic counselors reg...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2504&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis SUCLG2 Deletion/Duplication Analysis Test Code: 3963. Sequence & Deletion/Duplication Analysis SUCLG2 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3964. Sequence Analysis SUCLG2 Sequence Analysis Test Code: 3960. SUCLG2 Sequence Analysis Test Code: 3961 This test can only be performed if there is a previously identified familial mutation. SUCLG2 Sequence Analysis Test Code: 3962 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prio...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3963&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. LIG4 Related Disorders tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Next Generation Sequencing LIG4 Gene Sequencing by Massively Parallel Sequencing BCM-NGS SM. Test Code: 20505. Sequence Analysis. LIG4 Sequence Analysis Test Code: 20506 This test can only be performed if there is a previously identified familial mutation. LIG4 Sequence Analysis Test Code: 20507 We require that the referring center consult ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=20505
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. PHOX2B Related Disorders tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Next Generation Sequencing PHOX2B Gene Sequencing by Massively Parallel Sequencing BCM-NGS SM. Test Code: 22335. Sequence Analysis. PHOX2B Sequence Analysis Test Code: 22336 This test can only be performed if there is a previously identified familial mutation. PHOX2B Sequence Analysis Test Code: 22337 We require that the referring center ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=22335
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. PTCH1 Related Disorders tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Next Generation Sequencing PTCH1 Gene Sequencing by Massively Parallel Sequencing BCM-NGS SM. Test Code: 22340. Sequence Analysis. PTCH1 Sequence Analysis Test Code: 22341 This test can only be performed if there is a previously identified familial mutation. PTCH1 Sequence Analysis Test Code: 22342 We require that the referring center cons...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=22340
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. CDH1 Related Disorders tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Next Generation Sequencing CDH1 Gene Sequencing by Massively Parallel Sequencing BCM-NGS SM. Test Code: 22425. Sequence Analysis. CDH1 Sequence Analysis Test Code: 22426 This test can only be performed if there is a previously identified familial mutation. CDH1 Sequence Analysis Test Code: 22427 We require that the referring center consult ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=22425
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. CHEK2 Related Disorders tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Next Generation Sequencing CHEK2 Gene Sequencing by Massively Parallel Sequencing BCM-NGS SM. Test Code: 22430. Sequence Analysis. CHEK2 Sequence Analysis Test Code: 22431 This test can only be performed if there is a previously identified familial mutation. CHEK2 Sequence Analysis Test Code: 22432 We require that the referring center cons...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=22430
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. ATP6V0A2 Related Disorders tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Next Generation Sequencing ATP6V0A2 Gene Sequencing by Massively Parallel Sequencing BCM-NGS SM. Test Code: 29155. Sequence Analysis. ATP6V0A2 Sequence Analysis Test Code: 29156 This test can only be performed if there is a previously identified familial mutation. ATP6V0A2 Sequence Analysis Test Code: 29157 We require that the referring...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=29155
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. OPTN Related Disorders tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Next Generation Sequencing OPTN Gene Sequencing by Massively Parallel Sequencing BCM-NGS SM. Test Code: 29250. Sequence Analysis. OPTN Sequence Analysis Test Code: 29251 This test can only be performed if there is a previously identified familial mutation. OPTN Sequence Analysis Test Code: 29252 We require that the referring center consult ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=29250
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. FZD4 Related Disorders tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Next Generation Sequencing FZD4 Gene Sequencing by Massively Parallel Sequencing BCM-NGS SM. Test Code: 29255. Sequence Analysis. FZD4 Sequence Analysis Test Code: 29256 This test can only be performed if there is a previously identified familial mutation. FZD4 Sequence Analysis Test Code: 29257 We require that the referring center consult ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=29255
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Wolcott-Rallison Syndrome EIF2AK3 tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Next Generation Sequencing EIF2AK3 Gene Sequencing by Massively Parallel Sequencing BCM-NGS SM. Test Code: 21930. Sequence Analysis. EIF2AK3 Sequence Analysis Test Code: 21931 This test can only be performed if there is a previously identified familial mutation. EIF2AK3 Sequence Analysis Test Code: 21932 We require that the refer...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=21930
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. PLOD3 Related Disorders tests available. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis PLOD3 Deletion/Duplication Analysis Test Code: 2333. Sequence & Deletion/Duplication Analysis PLOD3 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2334. Sequence Analysis PLOD3 Sequence Analysis Test Code: 2330. PLOD3 Sequence Analysis Test Code: 2331 This test can only be performed if there is a previously identified familial mutation. PLOD3 Sequence Analysis Test Code: 2332 We require that the referring center consult with our laboratory genetic coun...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2333&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. RPGRIP1 Related Disorders tests available. RETINITIS PIGMENTOSA GTPase REGULATOR-INTERACTING PROTEIN Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis RPGRIP1 Deletion/Duplication Analysis Test Code: 2353. Next Generation Sequencing RPGRIP1 Gene Sequencing by Massively Parallel Sequencing BCM-NGS SM. Test Code: 32350. Sequence & Deletion/Duplication Analysis RPGRIP1 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2354. Sequence Analysis. RPGRIP1 Sequence Analysis Test Code: 2351 This test can only be performed if there is a previously identif...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2354&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. FAM20C Related Disorders tests available. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis FAM20C Deletion/Duplication Analysis Test Code: 2578. Sequence & Deletion/Duplication Analysis FAM20C Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2579. Sequence Analysis FAM20C Sequence Analysis Test Code: 2575. FAM20C Sequence Analysis Test Code: 2576 This test can only be performed if there is a previously identified familial mutation. FAM20C Sequence Analysis Test Code: 2577 We require that the referring center consult with our laboratory geneti...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2578&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis CA4 Deletion/Duplication Analysis Test Code: 2763. Sequence & Deletion/Duplication Analysis CA4 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2764. Sequence Analysis CA4 Sequence Analysis Test Code: 2760. CA4 Sequence Analysis Test Code: 2761 This test can only be performed if there is a previously identified familial mutation. CA4 Sequence Analysis Test Code: 2762 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2763&show=1
*  Medical Genetics Test Services - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, H
... ouston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Services View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. KARS-Related Intermediate Charcot-Marie-Tooth Neuropathy OMIM. KCNJ11 Related Disorders OMIM. KCNQ2 Related Disorders. Kennedy Disease OMIM GeneReview. Ketothiolase Deficiency ACAT1 OMIM. Ketotic Hypoglycemia and Gluconeogenesis Panel ALDOB, FBP1, GYS2, PC. KIF11-Related Disorders OMIM. KIT Exon 8 & 17 Mutation Analysis OMIM. KIT Exon 8, 9, 11, 13, 17 Mutation Analysis - Tumor - Non-FFPE. KIT Exon 8, 9, 11, 13,17 Mutation Analysis - Germline - Blood. KIT Exon 9 & 11 Mutation Analysis - Germline OMIM. KIT Exon 9 & 11 Mutation Analysis - Tumor OMIM. KLHL7-Related Retinitis...
https://bcm.edu/research/medical-genetics-labs/tests.cfm?browse=y&letter=K&cfid=320078617&cftoken=54819582
*  Medical Genetics Test Services - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, H
... ouston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Services View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. KARS-Related Intermediate Charcot-Marie-Tooth Neuropathy OMIM. KCNJ11 Related Disorders OMIM. KCNQ2 Related Disorders. Kennedy Disease OMIM GeneReview. Ketothiolase Deficiency ACAT1 OMIM. Ketotic Hypoglycemia and Gluconeogenesis Panel ALDOB, FBP1, GYS2, PC. KIF11-Related Disorders OMIM. KIT Exon 8 & 17 Mutation Analysis OMIM. KIT Exon 8, 9, 11, 13, 17 Mutation Analysis - Tumor - Non-FFPE. KIT Exon 8, 9, 11, 13,17 Mutation Analysis - Germline - Blood. KIT Exon 9 & 11 Mutation Analysis - Germline OMIM. KIT Exon 9 & 11 Mutation Analysis - Tumor OMIM. KLHL7-Related Retinitis...
https://bcm.edu/research/medical-genetics-labs/tests.cfm?browse=y&letter=K&cfid=340496615&cftoken=16548024
*  Medical Genetics Test Services - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, H
... ouston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Services View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. KARS-Related Intermediate Charcot-Marie-Tooth Neuropathy OMIM. KCNJ11 Related Disorders OMIM. KCNQ2 Related Disorders. Kennedy Disease OMIM GeneReview. Ketothiolase Deficiency ACAT1 OMIM. Ketotic Hypoglycemia and Gluconeogenesis Panel ALDOB, FBP1, GYS2, PC. KIF11-Related Disorders OMIM. KIT Exon 8 & 17 Mutation Analysis OMIM. KIT Exon 8, 9, 11, 13, 17 Mutation Analysis - Tumor - Non-FFPE. KIT Exon 8, 9, 11, 13,17 Mutation Analysis - Germline - Blood. KIT Exon 9 & 11 Mutation Analysis - Germline OMIM. KIT Exon 9 & 11 Mutation Analysis - Tumor OMIM. KLHL7-Related Retinitis...
https://bcm.edu/research/medical-genetics-labs/tests.cfm?browse=y&letter=K&cfid=340502588&cftoken=32313582
*  Medical Genetics Test Services - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, H
... ouston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Services View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. KARS-Related Intermediate Charcot-Marie-Tooth Neuropathy OMIM. KCNJ11 Related Disorders OMIM. KCNQ2 Related Disorders. Kennedy Disease OMIM GeneReview. Ketothiolase Deficiency ACAT1 OMIM. Ketotic Hypoglycemia and Gluconeogenesis Panel ALDOB, FBP1, GYS2, PC. KIF11-Related Disorders OMIM. KIT Exon 8 & 17 Mutation Analysis OMIM. KIT Exon 8, 9, 11, 13, 17 Mutation Analysis - Tumor - Non-FFPE. KIT Exon 8, 9, 11, 13,17 Mutation Analysis - Germline - Blood. KIT Exon 9 & 11 Mutation Analysis - Germline OMIM. KIT Exon 9 & 11 Mutation Analysis - Tumor OMIM. KLHL7-Related Retinitis...
https://bcm.edu/research/medical-genetics-labs/tests.cfm?browse=y&letter=K&cfid=340566816&cftoken=42051840
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis MFRP Deletion/Duplication Analysis Test Code: 2408. Sequence & Deletion/Duplication Analysis MFRP Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2409. Sequence Analysis MFRP Sequence Analysis Test Code: 2405. MFRP Sequence Analysis Test Code: 2406 This test can only be performed if there is a previously identified familial mutation. MFRP Sequence Analysis Test Code: 2407 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submi...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2408&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Glycogen storage disease XV GYG1 tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Next Generation Sequencing GYG1 Gene Sequencing by Massively Parallel Sequencing BCM-NGS SM. Test Code: 29035. Sequence Analysis. GYG1 Sequence Analysis Test Code: 29036 This test can only be performed if there is a previously identified familial mutation. GYG1 Sequence Analysis Test Code: 29037 We require that the referring cente...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=29035
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis RARS2 Deletion/Duplication Analysis Test Code: 3728. Sequence & Deletion/Duplication Analysis RARS2 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3729. Sequence Analysis RARS2 Sequence Analysis Test Code: 3725. RARS2 Sequence Analysis Test Code: 3726 This test can only be performed if there is a previously identified familial mutation. RARS2 Sequence Analysis Test Code: 3727 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3728&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. HPD Related Disorders tests available. Hawkinsinuria. Tyrosinemia type III Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Sequence Analysis HPD Sequence Analysis Test Code: 2075. HPD Sequence Analysis Test Code: 2076 This test can only be performed if there is a previously identified familial mutation. HPD Sequence Analysis Test Code: 2077 We require that the referring center consult with our laboratory genetic counselors reg...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2075&cfid=340563968&cftoken=92789176
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Peroxisome Biogenesis Disorder 6 PEX10 tests available. Peroxisome biogenesis disorder 6A Zellweger. Peroxisome biogenesis disorder 6B Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Next Generation Sequencing PEX10 Gene Sequencing by Massively Parallel Sequencing BCM-NGS SM. Test Code: 22140. Sequence Analysis. PEX10 Sequence Analysis Test Code: 22141 This test can only be performed if there is a previously identified familial mutation. PEX10 Sequence Analysis Test Code: 22142 We require...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=22140
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis MRPS22 Deletion/Duplication Analysis Test Code: 2288. Sequence & Deletion/Duplication Analysis MRPS22 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2289. Sequence Analysis MRPS22 Sequence Analysis Test Code: 2285. MRPS22 Sequence Analysis Test Code: 2286 This test can only be performed if there is a previously identified familial mutation. MRPS22 Sequence Analysis Test Code: 2287 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prio...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2288&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. RBP3-Related Retinitis Pigmentosa tests available. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis RBP3 Deletion/Duplication Analysis Test Code: 2463. Sequence & Deletion/Duplication Analysis RBP3 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2464. Sequence Analysis RBP3 Sequence Analysis Test Code: 2460. RBP3 Sequence Analysis Test Code: 2461 This test can only be performed if there is a previously identified familial mutation. RBP3 Sequence Analysis Test Code: 2462 We require that the referring center consult with our laboratory genetic...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2463&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Mitochondrial Complex III Deficiency-TTC19 Related tests available. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis TTC19 Deletion/Duplication Analysis Test Code: 2718. Sequence & Deletion/Duplication Analysis TTC19 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2719. Sequence Analysis TTC19 Sequence Analysis Test Code: 2715. TTC19 Sequence Analysis Test Code: 2716 This test can only be performed if there is a previously identified familial mutation. TTC19 Sequence Analysis Test Code: 2717 We require that the referring center consult with ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2718&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay GFER tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Next Generation Sequencing GFER Gene Sequencing by Massively Parallel Sequencing BCM-NGS SM. Test Code: 29010. Sequence Analysis. GFER Sequence Analysis Test Code: 29011 This test can only be performed if there is a previously identified familial mutation. GFER Seque...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=29010
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. MTFMT Related disorders tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Sequence Analysis MTFMT Sequence Analysis Test Code: 2235. MTFMT Sequence Analysis Test Code: 2236 This test can only be performed if there is a previously identified familial mutation. MTFMT Sequence Analysis Test Code: 2237 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2235
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. SNRNP200-Related Retinitis Pigmentosa tests available. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis SNRNP200 Deletion/Duplication Analysis Test Code: 2818. Sequence & Deletion/Duplication Analysis SNRNP200 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2819. Sequence Analysis SNRNP200 Sequence Analysis Test Code: 2815. SNRNP200 Sequence Analysis Test Code: 2816 This test can only be performed if there is a previously identified familial mutation. SNRNP200 Sequence Analysis Test Code: 2817 We require that the referring center consult wit...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2818&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Glycogen Storage Disease Type XI LDHA tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Sequence Analysis LDHA Sequence Analysis Test Code: 3785. LDHA Sequence Analysis Test Code: 3786 This test can only be performed if there is a previously identified familial mutation. LDHA Sequence Analysis Test Code: 3787 We require that the referring center consult with our laboratory genetic counselors regarding prenatal c...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3785&cfid=340563968&cftoken=92789176
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Severe Combined Immunodeficiency, B Cell-Negative tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Sequence Analysis RAG1 Sequence Analysis Test Code: 5295. RAG1 Sequence Analysis Test Code: 5296 This test can only be performed if there is a previously identified familial mutation. RAG1 Sequence Analysis Test Code: 5297 We require that the referring center consult with our laboratory genetic counselors regardin...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=5295
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Departments. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. GeneReviews Add to Custom Req. Print Req MAP2K2 Sequence Analysis Familial Mutation/Variant Analysis Test Information: Confirmation of Clinical Diagnosis - Known Familial Mutation s. Test Details Test Code: 6921. Test Includes: Sequencing of the region s containing the familial alteration s. Special Notes: This test can only be performed if there is a previously identified familial mutation. A laboratory report containing the relative's mutation information, the specific biological relationship of this patient and the tested relative and the clinical status of this patient symptomatic or asymptomatic must be submitted with the specimen. If the original familial mutation was identified in another...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=6921&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. DNA Replication Helicase/Nuclease 2 Deficiency, Metabolic Myopathy DNA2 tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Sequence Analysis DNA2 Sequence Analysis Test Code: 5160. DNA2 Sequence Analysis Test Code: 5161 This test can only be performed if there is a previously identified familial mutation. DNA2 Sequence Analysis Test Code: 5162 We require that the referring center consult with our laboratory genet...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=5160&cfid=329930367&cftoken=32630499
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. X-linked Immunodysregulation, Polyendocrinopathy, and Enteropathy FOXP3 tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Next Generation Sequencing FOXP3 Gene Sequencing by Massively Parallel Sequencing BCM-NGS SM. Test Code: 21935. Sequence Analysis. FOXP3 Sequence Analysis Test Code: 21936 This test can only be performed if there is a previously identified familial mutation. FOXP3 Sequence Analysis Test Code: 21937 We require that the referring center consult with our la...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=21935
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. NR2E3-Related Retinitis Pigmentosa tests available. RETINITIS PIGMENTOSA 37. RP37. PHOTORECEPTOR-SPECIFIC NUCLEAR RECEPTOR. PNR Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Sequence Analysis NR2E3 Sequence Analysis Test Code: 2905. NR2E3 Sequence Analysis Test Code: 2906 This test can only be performed if there is a previously identified familial mutation. NR2E3 Sequence Analysis Test Code: 2907 We require that the referrin...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2905&cfid=329930367&cftoken=32630499
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Citrin Deficiency SLC25A13 tests available. Neonatal Intrahepatic Cholestasis Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis SLC25A13 Deletion/Duplication Analysis Test Code: 3158. Sequence & Deletion/Duplication Analysis SLC25A13 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3159. Sequence Analysis SLC25A13 Sequence Analysis Test Code: 3155 Classic Citrullinemia is due to Argininosuccinate Synthase Deficiency see test codes #6180, #6185, #6190, #4542, #4543, #4544, #4545. SLC25A13 Sequence Analysis Test Code: 3156 This test can only be ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3155
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. MMACHC cblC - Related Disorders tests available. Methylmalonic Aciduria and Homocystinuria cblC type. cblC. Methylmalonic Acidemia and Homocystinuria cblC type. Disorders of Intracellular Cobalamin Metabolism Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis MMACHC Deletion/Duplication Analysis Test Code: 3443. Sequence & Deletion/Duplication Analysis MMACHC Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3444. Sequence Analysis MMACHC Sequence Analysis Test Code: 3440. MMACHC Sequence Analysis Test Code: 3441 This test can only ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3440
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Leber Congenital Amaurosis, Nicotinamide Nucleotide Adenylyltransferase 1 Deficiency NMNAT1 tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Sequence Analysis NMNAT1 Sequence Analysis Test Code: 5085. NMNAT1 Sequence Analysis Test Code: 5086 This test can only be performed if there is a previously identified familial mutation. NMNAT1 Sequence Analysis Test Code: 5087 We require that the referring center consult...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=5085
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions Autosomal Dominant 3. C10orf2 -Related Mitochondrial DNA Depletion Syndrome Hepatocerebral Form Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis C10orf2 TWINKLE Deletion/Duplication Analysis Test Code: 3178. Sequence & Deletion/Duplication Analysis C10orf2 TWINKLE Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3179. Sequence Analysis C10orf2 TWINKLE Sequence Analysis Test Code: 3175. C10orf2 TWINKLE Sequence Analysis Test Code: 3176 This test can only be performed if there is a previously identified familial mutation. Print Req C10orf2 TWINKLE Comp...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3179&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Tyrosinemia, Type 1 tests available. FAH Deficiency. Fumarylacetoacetase Deficiency. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Analyte Analysis Succinylacetone Determination - Urine Test Code: 4250 Succinylacetone is very labile. Deletion/Duplication Analysis FAH Deletion/Duplication Analysis Test Code: 3448. Sequence & Deletion/Duplication Analysis FAH Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3449. Sequence Analysis FAH Sequence Analysis Test Code: 3445. FAH Sequence Analysis Test Code: 3446 This test can only be performed if there is a previously identified familial mutation. FAH Sequence Analys...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3445&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Nuclear Encoded Complex I Deficiency - NDUFAF2 Related B17.2L, MMTN tests available. Mitochondrial Respiratory Chain Complex I Deficiency nuclear genes. Complex I. Mitochondrial Complex I Deficiency. Leigh Disease. Leigh Syndrome nuclear DNA mutation Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis NDUFAF2 Deletion/Duplication Analysis Test Code: 3538. Sequence & Deletion/Duplication Analysis NDUFAF2 Comprehensive - Sequence & Deletion/Duplication Analysis Test Co...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Nuclear Encoded Complex I Deficiency - NDUFS2-Related tests available. Mitochondrial Complex I Deficiency. Mitochondrial Respiratory Chain Complex I Deficiency nuclear genes. Complex I. Leigh Disease. Leigh Syndrome nuclear DNA mutation Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis NDUFS2 Deletion/Duplication Analysis Test Code: 3933. Sequence & Deletion/Duplication Analysis NDUFS2 Comprehensive - Sequence & Deletion/Duplication Analysis...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Transcobalamin II Deficiency TCN2 tests available. TC II Deficiency. TCN2 Deficiency Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis TCN2 Deletion/Duplication Analysis Test Code: 3968. Sequence & Deletion/Duplication Analysis TCN2 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3969. Sequence Analysis TCN2 Sequence Analysis Test Code: 3965. TCN2 Sequence Analysis Test Code: 3966 This test can only be performed if there is a previously identified familial mutation. TCN2 Sequence Analysis Test Code: 3967 We require that the referring center c...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. SCAD Deficiency ACADS tests available. Short Chain Acyl-CoA Dehydrogenase Deficiency. SCAD Deficiency Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis ACADS Deletion/Duplication Analysis Test Code: 3928. Sequence & Deletion/Duplication Analysis ACADS Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3929. Sequence Analysis ACADS Sequence Analysis Test Code: 3925. ACADS Sequence Analysis Test Code: 3926 This test can only be performed if there is a pr...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3925
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. SCAD Deficiency ACADS tests available. Short Chain Acyl-CoA Dehydrogenase Deficiency. SCAD Deficiency Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis ACADS Deletion/Duplication Analysis Test Code: 3928. Sequence & Deletion/Duplication Analysis ACADS Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3929. Sequence Analysis ACADS Sequence Analysis Test Code: 3925. ACADS Sequence Analysis Test Code: 3926 This test can only be performed if there is a pr...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3925&cfid=340563968&cftoken=92789176
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Fructose 1,6 Bisphosphatase Deficiency FBP1 tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis FBP1 Deletion/Duplication Analysis Test Code: 3938. Sequence & Deletion/Duplication Analysis FBP1 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3939. Sequence Analysis FBP1 Sequence Analysis Test Code: 3935. FBP1 Sequence Analysis Test Code: 3936 This test can only be performe...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3935&cfid=340563968&cftoken=92789176
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Niemann-Pick Disease Type C - NPC2 Related tests available. Juvenile Niemann-Pick Disease. Niemann-Pick Disease Type C2 Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Sequence Analysis NPC2 Sequence Analysis Test Code: 6560. NPC2 Sequence Analysis Test Code: 6561 This test can only be performed if there is a previously identified familial mutation. NPC2 Sequence Analysis Test Code: 6562 We require that the referring center co...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. FARS2 Related disorders tests available. Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis FARS2 Deletion/Duplication Analysis Test Code: 2248. Sequence & Deletion/Duplication Analysis FARS2 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2249. Sequence Analysis FARS2 Sequence Analysis Test Code: 2245. FARS2 Sequence Analysis Test Code: 2246 This test can only be performed if there is a previously identified familial mutation. FARS2 Sequence Analysis Test Code: 2247 We require that the referring center consult with our laboratory genetic coun...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Paget Disease, Juvenile TNFRSF11B tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis TNFRSF11B Deletion/Duplication Analysis Test Code: 2558. Sequence & Deletion/Duplication Analysis TNFRSF11B Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2559. Sequence Analysis TNFRSF11B Sequence Analysis Test Code: 2555. TNFRSF11B Sequence Analysis Test Code: 2556 This test can only b...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Mitochondrial Complex I Deficiency-FOXRED1 Related tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis FOXRED1 Deletion/Duplication Analysis Test Code: 2663. Sequence & Deletion/Duplication Analysis FOXRED1 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2664. Sequence Analysis FOXRED1 Sequence Analysis Test Code: 2660. FOXRED1 Sequence Analysis Test Code: 2661 This test c...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2660&cfid=340563968&cftoken=92789176
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Mitochondrial Complex I Deficiency-NDUFA11 Related tests available. Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis NDUFA11 Deletion/Duplication Analysis Test Code: 2683. Sequence & Deletion/Duplication Analysis NDUFA11 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2684. Sequence Analysis NDUFA11 Sequence Analysis Test Code: 2680. NDUFA11 Sequence Analysis Test Code: 2681 This test c...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2680
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. RDH12-Related Retinitis Pigmentosa tests available. RETINITIS PIGMENTOSA 53. RETINOL DEHYDROGENASE 12. RETINOL DEHYDROGENASE ALL-TRANS AND 9-CIS Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis RDH12 Deletion/Duplication Analysis Test Code: 2958. Sequence & Deletion/Duplication Analysis RDH12 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2959. Sequence Analysis RDH12 Sequence Analysis Test Code: 2955. RDH12 Sequence Analysis Test Code: 2956 This ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2955
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. CARNITINE PALMITOYLTRANSFERASE I MUSCLE. CPT I MUSCLE Click the blue dot to view test details. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis CPT1B Deletion/Duplication Analysis Test Code: 3373. Sequence & Deletion/Duplication Analysis CPT1B Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3374. Sequence Analysis CPT1B Sequence Analysis Test Code: 3370. CPT1B Sequence Analysis Test Code: 3371 This test can only be performed if there is a previously identified familial mutation. CPT1B Sequence Analysis Test Code: 3372 We require that the referring center consult with our laboratory...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3370&show=1
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Molybdenum Cofactor Deficiency - MOCS2 Related tests available. Combined Deficiency of Sulfite Oxidase Xanthine Dehydrogenase and Aldehyde Oxidase. Molybdopterin Synthase Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis MOCS2 Deletion/Duplication Analysis Test Code: 3618. Sequence & Deletion/Duplication Analysis MOCS2 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3619. Sequence Analysis MOCS2 Sequ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3615&cfid=329930367&cftoken=32630499
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. HNPCC - MLH1 Related tests available. Hereditary Non-Polyposis Colon Cancer. Lynch Syndrome. MLH1-Associated HNPCC. MLH1-Related Hereditary Non-Polyposis Colon Cancer. MLH1-Related Muir-Torre Syndrome. MLH1-Related Turcot Syndrome. Muir-Torre Syndrome. Turcot Syndrome Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis MLH1 Deletion/Duplication Analysis Test Code: 6706. MLH1 Deletion/Duplication Analysis Test Code: 6706. MLH1 Deletion/Duplication Analysis Test Code: 6706. Sequence & Deletion/...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=6705&cfid=329930367&cftoken=32630499
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Coenzyme Q10 Deficiency - COQ2 Related COQ2, CL640, FLJ26072 tests available. CoQ10. COQ2-Related Coenzyme Q10 Deficiency Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis COQ2 Deletion/Duplication Analysis Test Code: 3418. Sequence & Deletion/Duplication Analysis COQ2 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3419. Sequence Analysis COQ2 Sequence Analysis Test Code: 3415. COQ2 Sequence Analysis Test Code: 3416 This test can only be performed ...
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*  Medical Genetics Test Services - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, H
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*  Medical Genetics Test Services - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, H
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*  Medical Genetics Test Services - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, H
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*  Medical Genetics Test Services - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, H
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*  Medical Genetics Test Services - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, H
medical genetics test services baylor miraca genetics laboratories baylor college of medicine houston texas skip to content baylor miraca genetics laboratories genetic labs bcm home bcm centers bcm departments find a bcm person giving houston texas search baylor miraca genetics laboratories medical genetics test services view custom req tests in custom req search tests search by disease test name gene name test code or keyword return to test index browse a b c d e f g h i j k l m n o p q r s t u v w x y z jak exon mutation analysis omim jak v f mutation analysis omim home testing available test catalogue discontinued replaced tests reporting about us our licenses management team directors counselors billing institutional insurance international clients self pay pre payment chromosomal microarray prenatal testing financial cancellation contact information policies and forms forms requisitions consents authorizations shipping information shipping kits training programs resources array coverage search array publ...
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*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Nuclear Encoded Complex I Deficiency - NDUFS3 Related tests available. Mitochondrial Respiratory Chain Complex I Deficiency nuclear genes. Complex I. Mitochondrial Complex I Deficiency Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis NDUFS3 Deletion/Duplication Analysis Test Code: 3573. Sequence & Deletion/Duplication Analysis NDUFS3 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 3574. Sequence Analysis NDUFS3 Sequence Analysis Test Code: 3570. ND...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=3570&cfid=340563968&cftoken=92789176
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Ehlers-Danlos Syndrome, Classic Type - COL5A1 Related tests available. EDS Classic Type. Ehlers-Danlos Syndrome Type I. Ehlers-Danlos Syndrome Type II. Ehlers-Danlos Syndrome Classical Type Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Sequence Analysis COL5A1 Sequence Analysis Test Code: 6585. COL5A1 Sequence Analysis Test Code: 6586 This test can only be performed if there is a previously identified familial mutation. COL5A1 Sequence Analysis Test Code: 6587 We require that the referr...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=6585&cfid=340563968&cftoken=92789176
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Ehlers-Danlos Syndrome, Classic Type - COL5A2 Related tests available. EDS Classic Type. Ehlers-Danlos Syndrome Type I. Ehlers-Danlos Syndrome Type II. Ehlers-Danlos Syndrome Classical Type Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Sequence Analysis COL5A2 Sequence Analysis Test Code: 6590. COL5A2 Sequence Analysis Test Code: 6591 This test can only be performed if there is a previously identified familial mutation. COL5A2 Sequence Analysis Test Code: 6592 We require that the referr...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=6590&cfid=329930367&cftoken=32630499
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. PRPF6-Related Retinitis Pigmentosa tests available. RETINITIS PIGMENTOSA 60. RP60 Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis PRPF6 Deletion/Duplication Analysis Test Code: 2793. Sequence & Deletion/Duplication Analysis PRPF6 Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2794. Sequence Analysis PRPF6 Sequence Analysis Test Code: 2790. PRPF6 Sequence Analysis Test Code: 2791 This ...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2790&cfid=329930367&cftoken=32630499
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. LRAT-Related Retinitis Pigmentosa tests available. Retinitis pigmentosa juvenile. Retinal dystrophy early-onset severe Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Deletion/Duplication Analysis LRAT Deletion/Duplication Analysis Test Code: 2838. Sequence & Deletion/Duplication Analysis LRAT Comprehensive - Sequence & Deletion/Duplication Analysis Test Code: 2839. Sequence Analysis LRAT Sequence Analysis Test Code: 2835. LRAT Sequen...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=2835
*  Medical Genetics Test Details - Baylor Miraca Genetics Laboratories - Baylor College of Medicine, Ho
... uston, Texas. skip to content Baylor Miraca Genetics Laboratories Genetic Labs BCM Home. BCM Centers. BCM Departments. Find a BCM Person. Giving. Houston, Texas Search:. Baylor Miraca Genetics Laboratories. Medical Genetics Test Details View Custom Req. Tests in Custom Req: 0. Search Tests: Search by disease, test name, gene name, test code, or keyword. Return to test index. Browse: # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Obesity, Monogenic Nonsyndromic - PCSK1 Related tests available. Monogenic Non-Syndromic Obesity Autosomal Recessive. PCSK1 - Related Obesity Monogenic Nonsyndromic. Proprotein Convertase-1 Deficiency. Obesity and Endocrinopathy due to Impaired Processing of Prohormones Click the blue dot to view test details. Red dot = current test. Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing Sequence Analysis PCSK1 Sequence Analysis Test Code: 6855. PCSK1 Sequence Analysis Test Code: 6856 This test ca...
https://bcm.edu/research/medical-genetics-labs/test_detail.cfm?testcode=6855&cfid=340563968&cftoken=92789176

Walter Reed Army Institute of ResearchPanmixia: Panmixia (or panmixis) means random mating.King C and Stanfield W.David FulkerDda (DNA-dependent ATPase): Dda (short for DNA-dependent ATPase; also known as Dda helicase and Dda DNA helicase) is the 439-amino acid 49,897-atomic mass unit protein coded by the Dda gene of the bacteriophage T4 phage, a virus that infects enterobacteria.Genetic variation: right|thumbPhenotype microarray: The phenotype microarray approach is a technology for high-throughput phenotyping of cells.National Society of Film Critics Awards 1977: 12th NSFC AwardsSilent mutation: Silent mutations are mutations in DNA that do not significantly alter the phenotype of the organism in which they occur. Silent mutations can occur in non-coding regions (outside of genes or within introns), or they may occur within exons.Chromosome regionsGenetic linkage: Genetic linkage is the tendency of alleles that are located close together on a chromosome to be inherited together during the meiosis phase of sexual reproduction. Genes whose loci are nearer to each other are less likely to be separated onto different chromatids during chromosomal crossover, and are therefore said to be genetically linked.Return of results: Return of results is a concept in research ethics which describes the extent of the duty of a researcher to reveal and explain the results of research to a research participant.Population stratification: Population stratification is the presence of a systematic difference in allele frequencies between subpopulations in a population possibly due to different ancestry, especially in the context of association studies. Population stratification is also referred to as population structure, in this context.Infinite alleles model: The infinite alleles model is a mathematical model for calculating genetic mutations. The Japanese geneticist Motoo Kimura and American geneticist James F.Ontario Genomics Institute: The Ontario Genomics Institute (OGI) is a not-for-profit organization that manages cutting-edge genomics research projects and platforms.The Ontario Genomics Institute OGI also helps scientists find paths to the marketplace for their discoveries and the products to which they lead, and it works through diverse outreach and educational activities to raise awareness and facilitate informed public dialogue about genomics and its social impacts.WGAViewer: WGAViewer is a bioinformatics software tool which is designed to visualize, annotate, and help interpret the results generated from a genome wide association study (GWAS). Alongside the P values of association, WGAViewer allows a researcher to visualize and consider other supporting evidence, such as the genomic context of the SNP, linkage disequilibrium (LD) with ungenotyped SNPs, gene expression database, and the evidence from other GWAS projects, when determining the potential importance of an individual SNP.Eugenics in the United States: Eugenics, the set of beliefs and practices which aims at improving the genetic quality of the human population played a significant role in the history and culture of the United States prior to its involvement in World War II.Hereditary Disease Foundation: The Hereditary Disease Foundation (HDF) aims to cure genetic disorders by supporting basic biomedical research.Microsatellite: A microsatellite is a tract of repetitive DNA in which certain DNA motifs (ranging in length from 2–5 base pairs) are repeated, typically 5-50 times. Microsatellites occur at thousands of locations in the human genome and they are notable for their high mutation rate and high diversity in the population.Selection (relational algebra): In relational algebra, a selection (sometimes called a restriction to avoid confusion with SQL's use of SELECT) is a unary operation written asGene polymorphismDNA sequencer: A DNA sequencer is a scientific instrument used to automate the DNA sequencing process. Given a sample of DNA, a DNA sequencer is used to determine the order of the four bases: G (guanine), C (cytosine), A (adenine) and T (thymine).Molecular evolution: Molecular evolution is a change in the sequence composition of cellular molecules such as DNA, RNA, and proteins across generations. The field of molecular evolution uses principles of evolutionary biology and population genetics to explain patterns in these changes.Coles PhillipsBernd BrinkmannUniparental inheritance: Uniparental inheritance is a non-mendelian form of inheritance that consists of the transmission of genotypes from one parental type to all progeny. That is, all the genes in offspring will originate from only the mother or only the father.Branching order of bacterial phyla (Gupta, 2001): There are several models of the Branching order of bacterial phyla, one of these was proposed in 2001 by Gupta based on conserved indels or protein, termed "protein signatures", an alternative approach to molecular phylogeny. Some problematic exceptions and conflicts are present to these conserved indels, however, they are in agreement with several groupings of classes and phyla.Pedigree chart: A pedigree chart is a diagram that shows the occurrence and appearance or phenotypes of a particular gene or organism and its ancestors from one generation to the next,pedigree chart Genealogy Glossary - About.com, a part of The New York Times Company.Cancer Genome Project: The Cancer Genome Project, based at the Wellcome Trust Sanger Institute, aims to identify sequence variants/mutations critical in the development of human cancers. Like The Cancer Genome Atlas project within the United States, the Cancer Genome Project represents an effort in the War on Cancer to improve cancer diagnosis, treatment, and prevention through a better understanding of the molecular basis of this disease.Pharmacogenetics: Pharmacogenetics is the study of inherited genetic differences in drug metabolic pathways which can affect individual responses to drugs, both in terms of therapeutic effect as well as adverse effects. The term pharmacogenetics is often used interchangeably with the term pharmacogenomics which also investigates the role of acquired and inherited genetic differences in relation to drug response and drug behavior through a systematic examination of genes, gene products, and inter- and intra-individual variation in gene expression and function.Evolution in Variable EnvironmentExtracellular: In cell biology, molecular biology and related fields, the word extracellular (or sometimes extracellular space) means "outside the cell". This space is usually taken to be outside the plasma membranes, and occupied by fluid.Michael K. Denk: Michael K. Denk (or Karl Michael Denk) is a Professor of chemistry at the University of Guelph, Ontario.Symmetry element: A symmetry element is a point of reference about which symmetry operations can take place. In particular, symmetry elements can be centers of inversion, axes of rotation and mirror planes.Deterministic system (philosophy): A deterministic system is a conceptual model of the philosophical doctrine of determinism applied to a system for understanding everything that has and will occur in the system, based on the physical outcomes of causality. In a deterministic system, every action, or cause, produces a reaction, or effect, and every reaction, in turn, becomes the cause of subsequent reactions.Genetic predisposition: A genetic predisposition is a genetic characteristic which influences the possible phenotypic development of an individual organism within a species or population under the influence of environmental conditions. In medicine, genetic susceptibility to a disease refers to a genetic predisposition to a health problem,What does it mean to have a genetic predisposition to a disease?Recombination (cosmology): In cosmology, recombination refers to the epoch at which charged electrons and protons first became bound to form electrically neutral hydrogen atoms.Note that the term recombination is a misnomer, considering that it represents the first time that electrically neutral hydrogen formed.Disequilibrium (medicine): Disequilibrium}}The Flash ChroniclesTrisomic rescue: Trisomic rescue (also known as trisomy rescue or trisomy zygote rescue) is a genetic phenomenon in which a fertilized ovum containing three copies of a chromosome loses one of these chromosomes to form a normal, diploid chromosome complement. If both of the retained chromosomes came from the same parent, then uniparental disomy results.Hybrid inviability: Hybrid inviability is a post-zygotic barrier, which reduces a hybrid's capacity to mature into a healthy, fit adult.Hybrid inviability.List of sequenced eukaryotic genomesDrosophila embryogenesis: Drosophila embryogenesis, the process by which Drosophila (fruit fly) embryos form, is a favorite model system for geneticists and developmental biologists studying embryogenesis. The small size, short generation time, and large brood size make it ideal for genetic studies.Plant breedingIndy (gene): Indy, short for I'm not dead yet, is a gene of the model organism, the fruit fly Drosophila melanogaster. Mutant versions of this gene have doubled the average life span of fruit flies in at least one set of experiments, but this result has been subject to controversy.Haplogroup L0 (mtDNA)Genetic heterogeneity: Genetic heterogeneity is a phenomenon in which a single phenotype or genetic disorder may be caused by any one of a multiple number of alleles or non-allele (locus) mutations.Turnpenny and Ellard, Emery's Elements of Medical Genetics, 13th Edition.Matrix model: == Mathematics and physics ==PSI Protein Classifier: PSI Protein Classifier is a program generalizing the results of both successive and independent iterations of the PSI-BLAST program. PSI Protein Classifier determines belonging of the found by PSI-BLAST proteins to the known families.Mac OS X Server 1.0Health geography: Health geography is the application of geographical information, perspectives, and methods to the study of health, disease, and health care.Chromosome engineering: Chromosome engineering is "the controlled generation of chromosomal deletions, inversions, or translocations with defined endpoints." For: By combining chromosomal translocation, chromosomal inversion,and chromosomal deletion, chromosome engineering has been shown to identify the underlying genes that cause certain diseases in mice.Gross pathology: Gross pathology refers to macroscopic manifestations of disease in organs, tissues, and body cavities. The term is commonly used by anatomical pathologists to refer to diagnostically useful findings made during the gross examination portion of surgical specimen processing or an autopsy.Reproductive toxicity: Reproductive toxicity is a hazard associated with some chemical substances, that they will interfere in some way with normal reproduction; such substances are called reprotoxic. It includes adverse effects on sexual function and fertility in adult males and females, as well as developmental toxicity in the offspring.Inbreeding depression: Inbreeding depression is the reduced biological fitness in a given population as a result of inbreeding, or breeding of related individuals. Population biological fitness refers to its ability to survive and reproduce itself.Microevolution: Microevolution is the change in allele frequencies that occur over time within a population.Microevolution: What is microevolution?Protein primary structure: The primary structure of a peptide or protein is the linear sequence of its amino acid structural units, and partly comprises its overall biomolecular structure. By convention, the primary structure of a protein is reported starting from the amino-terminal (N) end to the carboxyl-terminal (C) end.QRISK: QRISK2 (the most recent version of QRISK) is a prediction algorithm for cardiovascular disease (CVD) that uses traditional risk factors (age, systolic blood pressure, smoking status and ratio of total serum cholesterol to high-density lipoprotein cholesterol) together with body mass index, ethnicity, measures of deprivation, family history, chronic kidney disease, rheumatoid arthritis, atrial fibrillation, diabetes mellitus, and antihypertensive treatment.Acromelanism: Acromelanism is a genetically determined, temperature-dependent pigmentation pattern, with full expression only occurring on legs, ears, tail and face. Seen in Siamese and Himalayan cats, rats, and rabbits.Nutrigenetics: Nutrigenetics is a branch of nutritional genomics which aims to identify genetic susceptibility to diseases and genetic variation in the effects of nutrient intake on the genome. Nutrigenetics is not to be confused with nutrigenomics, which focuses on the role specific foods have in activating genes that affect susceptibility to certain illnesses such as Alzheimer’s Disease and cancer.Interval boundary element method: Interval boundary element method is classical boundary element method with the interval parameters.
Newington Green Unitarian ChurchThe Otwell Twins: The Otwell Twins are an American singing duo made up of identical twin brothers Roger and David, born August 2, 1956, in Tulia, Texas. They are best known as members of The Lawrence Welk Show from 1977-1982.Gene signature: A gene signature is a group of genes in a cell whose combined expression patternItadani H, Mizuarai S, Kotani H. Can systems biology understand pathway activation?OpsismodysplasiaClonal Selection Algorithm: In artificial immune systems, Clonal selection algorithms are a class of algorithms inspired by the clonal selection theory of acquired immunity that explains how B and T lymphocytes improve their response to antigens over time called affinity maturation. These algorithms focus on the Darwinian attributes of the theory where selection is inspired by the affinity of antigen-antibody interactions, reproduction is inspired by cell division, and variation is inspired by somatic hypermutation.

(1/6490) An overview of the evolution of overproduced esterases in the mosquito Culex pipiens.

Insecticide resistance genes have developed in a wide variety of insects in response to heavy chemical application. Few of these examples of adaptation in response to rapid environmental change have been studied both at the population level and at the gene level. One of these is the evolution of the overproduced esterases that are involved in resistance to organophosphate insecticides in the mosquito Culex pipiens. At the gene level, two genetic mechanisms are involved in esterase overproduction, namely gene amplification and gene regulation. At the population level, the co-occurrence of the same amplified allele in distinct geographic areas is best explained by the importance of passive transportation at the worldwide scale. The long-term monitoring of a population of mosquitoes in southern France has enabled a detailed study to be made of the evolution of resistance genes on a local scale, and has shown that a resistance gene with a lower cost has replaced a former resistance allele with a higher cost.  (+info)

(2/6490) Evolutionary analysis of TATA-less proximal promoter function.

Many molecular studies describe how components of the proximal promoter affect transcriptional processes. However, these studies do not account for the likely effects of distant enhancers or chromatin structure, and thus it is difficult to conclude that the sequence variation in proximal promoters acts to modulate transcription in the natural context of the whole genome. This problem, the biological importance of proximal promoter sequence variation, can be addressed using a combination of molecular and evolutionary analyses. Provided here are molecular and evolutionary analyses of the variation in promoter function and sequence within and between populations of Fundulus heteroclitus for the lactate dehydrogenase-B (Ldh-B) proximal promoter. Approximately one third of the Ldh-B proximal promoter contains interspersed regions that are functionally important: (1) they bind transcription factors in vivo, (2) they effect a change in transcription as assayed by transient transfection into two different fish cell lines, and (3) they bind purified transcription factors in vitro. Evolutionary analyses that compare sequence variation in these functional regions versus the nonfunctional regions indicate that the changes in the Ldh-B proximal promoter sequences are due to directional selection. Thus, the Ldh-B proximal promoter sequence variations that affect transcriptional processes constitute a phenotypic change that is subject to natural selection, suggesting that proximal promoter sequence variation affects transcription in the natural context of the whole genome.  (+info)

(3/6490) Ancestral Asian source(s) of new world Y-chromosome founder haplotypes.

Haplotypes constructed from Y-chromosome markers were used to trace the origins of Native Americans. Our sample consisted of 2,198 males from 60 global populations, including 19 Native American and 15 indigenous North Asian groups. A set of 12 biallelic polymorphisms gave rise to 14 unique Y-chromosome haplotypes that were unevenly distributed among the populations. Combining multiallelic variation at two Y-linked microsatellites (DYS19 and DXYS156Y) with the unique haplotypes results in a total of 95 combination haplotypes. Contra previous findings based on Y- chromosome data, our new results suggest the possibility of more than one Native American paternal founder haplotype. We postulate that, of the nine unique haplotypes found in Native Americans, haplotypes 1C and 1F are the best candidates for major New World founder haplotypes, whereas haplotypes 1B, 1I, and 1U may either be founder haplotypes and/or have arrived in the New World via recent admixture. Two of the other four haplotypes (YAP+ haplotypes 4 and 5) are probably present because of post-Columbian admixture, whereas haplotype 1G may have originated in the New World, and the Old World source of the final New World haplotype (1D) remains unresolved. The contrasting distribution patterns of the two major candidate founder haplotypes in Asia and the New World, as well as the results of a nested cladistic analysis, suggest the possibility of more than one paternal migration from the general region of Lake Baikal to the Americas.  (+info)

(4/6490) X chromosome evidence for ancient human histories.

Diverse African and non-African samples of the X-linked PDHA1 (pyruvate dehydrogenase E1 alpha subunit) locus revealed a fixed DNA sequence difference between the two sample groups. The age of onset of population subdivision appears to be about 200 thousand years ago. This predates the earliest modern human fossils, suggesting the transformation to modern humans occurred in a subdivided population. The base of the PDHA1 gene tree is relatively ancient, with an estimated age of 1.86 million years, a late Pliocene time associated with early species of Homo. PDHA1 revealed very low variation among non-Africans, but in other respects the data are consistent with reports from other X-linked and autosomal haplotype data sets. Like these other genes, but in conflict with microsatellite and mitochondrial data, PDHA1 does not show evidence of human population expansion.  (+info)

(5/6490) Maximum-likelihood generalized heritability estimate for blood pressure in Nigerian families.

Elevated blood pressure (BP) is more common in relatives of hypertensives than in relatives of normotensives, indicating familial resemblance of the BP phenotypes. Most published studies have been conducted in westernized societies. To assess the ability to generalize these estimates, we examined familial patterns of BP in a population-based sample of 510 nuclear families, including 1552 individuals (320 fathers, 370 mothers, 475 sons, and 387 daughters) from Ibadan, Nigeria. The prevalence of obesity in this community is low (body mass index: fathers, 21.6; mothers, 23.6; sons, 19.2; and daughters=21.0 kg/m2). The BP phenotype used in all analyses was created from the best regression model by standardizing the age-adjusted systolic blood pressure (SBP) and diastolic blood pressure (DBP) to 0 mean and unit variance. Heritability was estimated by use of the computer program SEGPATH from the most parsimonious model of "no spouse and neither gender nor generation difference" as 45% for SBP and 43% for DBP. The lack of a significant spouse correlation is consistent with little or no influence of the common familial environment. However, the heritability estimate of <50% for both SBP and DBPs reinforces the importance of the nonshared environmental effect.  (+info)

(6/6490) DnaSP version 3: an integrated program for molecular population genetics and molecular evolution analysis.

DnaSP is a Windows integrated software package for the analysis of the DNA polymorphism from nucleotide sequence data. DnaSP version 3 incorporates several methods for estimating the amount and pattern of DNA polymorphism and divergence, and for conducting neutrality tests. AVAILABILITY: For academic uses, DnaSP is available free of charge from: http://www.bio.ub.es/julio/DnaSP.html CONTACT: julio@porthos.bio.ub.es  (+info)

(7/6490) Early medieval cattle remains from a Scandinavian settlement in Dublin: genetic analysis and comparison with extant breeds.

A panel of cattle bones excavated from the 1000-year-old Viking Fishamble Street site in Dublin was assessed for the presence of surviving mitochondrial DNA (mtDNA). Eleven of these bones gave amplifiable mtDNA and a portion of the hypervariable control region was determined for each specimen. A comparative analysis was performed with control region sequences from five extant Nordic and Irish cattle breeds. The medieval population displayed similar levels of mtDNA diversity to modern European breeds. However, a number of novel mtDNA haplotypes were also detected in these bone samples. In addition, the presence of a putative ancestral sequence at high frequency in the medieval population supports an early post-domestication expansion of cattle in Europe.  (+info)

(8/6490) Freezer anthropology: new uses for old blood.

Archived blood fractions (plasma, settled red cells, white cells) have proved to be a rich and valuable source of DNA for human genetic studies. Large numbers of such samples were collected between 1960 and the present for protein and blood group studies, many of which are languishing in freezers or have already been discarded. More are discarded each year because the usefulness of these samples is not widely understood. Data from DNA derived from 10-35-year-old blood samples have been used to address the peopling of the New World and of the Pacific. Mitochondrial DNA haplotypes from studies using this source DNA support a single wave of migration into the New World (or a single source population for the New World), and that Mongolia was the likely source of the founding population. Data from Melanesia have shown that Polynesians are recent immigrants into the Pacific and did not arise from Melanesia.  (+info)


How does genetics and muscle growth work?


Does genetics really play a role in muscle and growth? Will my child have genetics to get muscle easier because I work out and have lots muscles? My parents, grand parents, great grandparents all had no muscle. I'm confused, how does genetics and muscles work?
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I think he maybe be a little bit more prone to getting muscles because of you directly but stuff stays in the genes for a very very long time. but genetics and muscles means some muscles will develop easier than others...


How much does your genetics affect with becoming bigger and gaining muscle?


Unfortunately I was born with some pretty shitty genetics.  Pretty much everyone in my family has really skinny wrists and arms and is bigger in the stomach area.  I've been working out quite a bit for the past 4 months now and I really haven't gotten much bigger and I see some pretty big dudes at the gym and was just wondering is it your genetics that determines how big you can get?
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Yes, but it doesn't sound like you are limited by your genetics at this point. Maybe after you put on 50-70 pounds of muscle, you may be limited, but not right now. Your limited by your workouts and your diet. Do some research, go on bodybuilding.com and click on "supersite." Learn how to eat, how much protein you should be eating, how often, etc... And ONLY do workouts if they are in a magazine or if you got them online. Also, workout 5 days a week. No full body or upperbody then lower body workouts either. No swinging your body or letting your ego take over, no cheating, ONLY use a weight you can control at all times. Its not your genetics at this point, no way


How much does Genetics have to do with muscle growth?


I don't have the best family genetics, but i train at the gym, and train very hard. I am a 17 yr old male, I have a four pack somewhat and pretty, well ok defined muscle. But i was wondering how much genetics really had to do with muscle growth and getting a six pack and what not?
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Not as much as a lot of people may think. So not all that much. It comes down to how motivated you are to build muscle.


What population of people have a caffeine addiction?


I need to know what type of population has caffeine addictions and what the treatment plan is.
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Depends on how you define addiction. 

If addiction is defined by withdrawal symptoms, then as an above poster said, 90% is a fair estimate of the caffeine drinking population worldwide, if you include milder versions like green tea in the East, and these people would likely all experience some degree of withdrawal if caffeine were withheld. 

If addiction is defined by the consequences of the substance use, then you'd have to make the case that a caffeine addict suffers relationship problems, money problems, and other addiction related consequences due to their consumption of caffeine.


When the government introduces population control, how will it work?


It's going to happen sooner or later with global warming, as global over-population is one of the major contributing factors to climate change.

What would be the criteria involved in having children? Should there be genetic screening first? How would population control be enforced? Through the tax system?
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Yes if I had that power I would make these rules..

•Put a limit of two children to every couple...If you exceed the limit after the year 2009 you will pay a tax....I think the rule of one child in China is to harsh.
•If one of your children dies you can fill their place with another pregnancy.
•People will be paid if they adopt instead of having biological children.
•Make BC free.
•Try to get other nations to take up the law.
•This way the children don't out number the parents...over time if it were enforced everywhere would hopefully reduce the population of the world.

•AND I would also do several things to help the enviroment anyway.


If the world population is increasing how do vegetarians hope to make a difference?


If the population is increasing how do vegetarians hope to make a difference when they hold a small small minority of the world population, obviously it is better to attempt to help. But is yer choice of being a vegetarian due to the moral ethics (ie you don't agree with the standard that meat is procured etc & feel less ''sinful'' by avoiding it) 
or are you trying to make a difference through activism or denying yourself meat?
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Well, I don't like smoking cigarettes, so I don't do that either. Will I single-handedly put the entire tobacco industry to rest simply by avoiding their products? No, and I feel the same way about meat. I like animals and I take them seriously enough to not eat them. I don't need their flesh to survive, so I would rather take the ethical high-road and do what I feel is right. I don't expect to make a big difference, but the least I can say for myself is that I am not directly or purposefully contributing to the exploitation of animals. :)


How much does genetics play in building body mass?


I have friends who put on size easily.  I, on the other hand, have always been skinny.  I've noticed that I've been gaining some weight as of recently.  I wanted to know if I can build muscle mass just like any other person that goes to the gym or does genetics pretty much say yes or no to more muscles?
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I would say genetics plays a significant part. You will build muscle a different rate than your friend. It may be harder or easier. I would suggest asking your dad if it was hard for him to put on muscle and this may give you an idea, but may not be completely true for you.


What percentage of the population upstream has their urine drunk by lowerstream populations?


The water we drink comes from upstream places. I would like to know what proportion of the upstream population's urine we drink. This is the water that comes from sewage treatment plants.
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There is no urine in the water you drink except possible on the molecule level.  It would not be detectable, except after an accident.  The water is purified before being put back in the river.  Depending on the place we are talking about you could be drinking water resulting from the use by >95% of the people.  It would include all household uses including the water from bathing, washing, and laundry.  See the references on how it works.  There would be a greater amount of animal urine than human when they take it out of the river.  Again, before use, it is purified again.