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Anatomy43

X Chromosome Brain Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 11 Heart Nerve Fibers, Myelinated Chromosomes, Human, Pair 7 Cells, Cultured Cerebral Cortex Corpus Callosum Chromosomes, Human, Pair 18 Chromosomes, Human, Pair 17 Heart Ventricles Spermatozoa Bone Marrow Kidney Lung Liver Myocardium Fetus Chromosomes, Human, Pair 14 Cerebellum Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 1 Skin Bone and Bones Chromosomes, Human, 6-12 and X Temporal Lobe Embryo, Mammalian Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 12 Neurons Frontal Lobe Chromosomes, Human, Pair 21 Cell Line Skull Chromosomes, Human, X Retina Chromosomes, Human, Pair 6 Chromosomes, Human, 13-15 Cerebral Ventricles Chromosomes, Human

Organisms9

Mice, Knockout Mice, Inbred C57BL Mice, Transgenic Mice, Mutant Strains Animals, Newborn Dogs Bacteriophage phi X 174 Rats, Sprague-Dawley Mice, Neurologic Mutants

Diseases71

Genetic Predisposition to Disease Alcoholism Abnormalities, Multiple Chromosome Aberrations Congenital Abnormalities Chromosome Disorders Eye Abnormalities Cardiovascular Abnormalities Craniofacial Abnormalities Syndrome Skin Abnormalities Trisomy Urogenital Abnormalities Musculoskeletal Abnormalities Tooth Abnormalities Translocation, Genetic Aneuploidy Disease Models, Animal Sex Chromosome Aberrations Abnormalities, Drug-Induced Fetal Diseases Brain Diseases Chromosome Deletion Heart Defects, Congenital Intellectual Disability Nervous System Malformations Down Syndrome Agenesis of Corpus Callosum Digestive System Abnormalities Atrophy Limb Deformities, Congenital Infertility, Male Ocular Motility Disorders Myelodysplastic Syndromes Blood Coagulation Disorders Abnormal Karyotype Heart Diseases Acute Disease Turner Syndrome Nervous System Diseases Disease Progression Monosomy Arrhythmias, Cardiac Cardiomyopathies Retinal Diseases Sturge-Weber Syndrome Maxillofacial Abnormalities Respiratory System Abnormalities Body Weight Jaw Abnormalities Chronic Disease Fetal Death Epilepsy Metabolic Diseases Leukemia, Myeloid, Acute Hypertension Microcephaly Seizures Ventricular Dysfunction, Left Eye Diseases Sensation Disorders Bone Diseases, Developmental Mouth Abnormalities Malformations of Cortical Development Foot Deformities, Congenital Growth Disorders Movement Disorders Recurrence Vision Disorders Blood Platelet Disorders Leukemia, Myeloid

Chemicals and Drugs12

Serotonin Plasma Membrane Transport Proteins Factor X RNA, Messenger Retinoid X Receptors Biological Markers Transcription Factors DNA-Binding Proteins Nerve Tissue Proteins Blood Glucose DNA Insulin Membrane Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment62

Genetic Association Studies Models, Genetic Risk Factors Karyotyping Magnetic Resonance Imaging In Situ Hybridization, Fluorescence Disease Models, Animal Electrocardiography Retrospective Studies Case-Control Studies Pedigree Prospective Studies Cytogenetic Analysis Sensitivity and Specificity Tomography, X-Ray Computed Chromosome Banding Ultrasonography, Prenatal Follow-Up Studies Prenatal Diagnosis Prognosis Reference Values Echocardiography Predictive Value of Tests Biopsy Electroencephalography Analysis of Variance Immunohistochemistry Neurologic Examination Reproducibility of Results Diffusion Magnetic Resonance Imaging Polymerase Chain Reaction Treatment Outcome Severity of Illness Index Cohort Studies DNA Mutational Analysis Chromosome Mapping Prevalence Tomography, Emission-Computed, Single-Photon Microscopy, Electron Gene Targeting Diffusion Tensor Imaging Brain Mapping Electroretinography Organ Size Amniocentesis Radiography, Thoracic Body Weight Crosses, Genetic Blood Pressure Observer Variation Echoencephalography Imaging, Three-Dimensional Ultrasonography Statistics, Nonparametric In Situ Hybridization Vaginal Smears Chi-Square Distribution Autopsy Leukocyte Count Cross-Sectional Studies Magnetic Resonance Angiography Incidence

Psychiatry and Psychology12

Adult Children Life Change Events Alcoholism Schizophrenia Intellectual Disability Neuropsychological Tests Developmental Disabilities Autistic Disorder Dominance, Cerebral Cognition Disorders Behavior, Animal Functional Laterality

Phenomena and Processes75

Gene-Environment Interaction Epistasis, Genetic Environment Genetic Predisposition to Disease Genotype Phenotype Polymorphism, Single Nucleotide Alleles Polymorphism, Genetic Chromosome Aberrations X Chromosome Mutation Trisomy Pregnancy Translocation, Genetic Time Factors Aneuploidy Sex Chromosome Aberrations Sensitivity and Specificity Chromosome Deletion Heterozygote Homozygote Base Sequence Chromosomes, Human, Pair 13 Mosaicism Chromosomes, Human, Pair 11 Gene Deletion Gestational Age Abnormal Karyotype Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 18 Anisotropy Monosomy Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 14 Amino Acid Sequence Aging Organ Size Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 1 Body Weight Gene Expression Chromosomes, Human, 6-12 and X Gene Expression Regulation, Developmental Dominance, Cerebral Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 3 Genes, Recessive Chromosomes, Human, Pair 12 Neural Conduction Signal Transduction Blood Pressure Myocardial Contraction Gene Rearrangement Chromosomes, Human, Pair 21 Dose-Response Relationship, Drug Embryonic and Fetal Development Ploidies Functional Laterality Chromosomes, Human, X Gene Expression Regulation Chromosomes, Human, Pair 6 Pregnancy Trimester, Second Chromosomes, Human, 13-15 Mutation, Missense Genetic Linkage Chi-Square Distribution Gene Dosage Point Mutation Cell Differentiation Leukocyte Count Chromosomes, Human Exons Genes, Dominant Hemodynamics

Disciplines and Occupations2

Cytogenetics Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena3

Adult Children Social Environment Autopsy

Information Science7

Image Processing, Computer-Assisted Molecular Sequence Data Base Sequence Prevalence Amino Acid Sequence Imaging, Three-Dimensional Incidence

Named Groups2

Adult Children Infant, Newborn

Health Care20

Environment Risk Factors Retrospective Studies Case-Control Studies Prospective Studies Sensitivity and Specificity Follow-Up Studies Predictive Value of Tests Analysis of Variance Reproducibility of Results Treatment Outcome Severity of Illness Index Cohort Studies Age Factors Prevalence Observer Variation Statistics, Nonparametric Chi-Square Distribution Cross-Sectional Studies Incidence

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care

Gene-Environment Interaction Serotonin Plasma Membrane Transport Proteins Epistasis, Genetic Adult Children Environment Genetic Predisposition to Disease Genotype Phenotype Social Environment Genetic Association Studies Polymorphism, Single Nucleotide Models, Genetic Life Change Events Alleles Polymorphism, Genetic Alcoholism Abnormalities, Multiple Chromosome Aberrations X Chromosome Risk Factors Congenital Abnormalities Chromosome Disorders Karyotyping Eye Abnormalities Magnetic Resonance Imaging Brain Cardiovascular Abnormalities Craniofacial Abnormalities Syndrome Mutation Skin Abnormalities Trisomy Urogenital Abnormalities In Situ Hybridization, Fluorescence Pregnancy Factor X Musculoskeletal Abnormalities Tooth Abnormalities Translocation, Genetic Time Factors Aneuploidy Infant, Newborn Disease Models, Animal Electrocardiography Retrospective Studies Case-Control Studies Pedigree Sex Chromosome Aberrations Abnormalities, Drug-Induced Prospective Studies Fetal Diseases Mice, Knockout Cytogenetic Analysis Schizophrenia Sensitivity and Specificity Tomography, X-Ray Computed Brain Diseases Chromosome Deletion Chromosome Banding Ultrasonography, Prenatal Mice, Inbred C57BL Image Processing, Computer-Assisted Heart Defects, Congenital Follow-Up Studies Heterozygote Prenatal Diagnosis Mice, Transgenic Cytogenetics Molecular Sequence Data Intellectual Disability Homozygote Prognosis Nervous System Malformations Reference Values Echocardiography Mice, Mutant Strains Base Sequence Chromosomes, Human, Pair 13 Mosaicism Predictive Value of Tests Biopsy Down Syndrome Agenesis of Corpus Callosum Electroencephalography Analysis of Variance Digestive System Abnormalities Atrophy Chromosomes, Human, Pair 11 Limb Deformities, Congenital Heart Immunohistochemistry Gene Deletion Neurologic Examination Gestational Age Infertility, Male Reproducibility of Results Ocular Motility Disorders Diffusion Magnetic Resonance Imaging Myelodysplastic Syndromes Polymerase Chain Reaction

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