Gene mutations genes x linked. Medical search. Frequent questions

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Anatomy9

X Chromosome Cell Line COS Cells Cells, Cultured Chromosomes, Human, Pair 17 Cell Line, Tumor Fibroblasts Tumor Cells, Cultured HEK293 Cells

Organisms11

Escherichia coli Saccharomyces cerevisiae Oxytropis Mice, Mutant Strains Mice, Transgenic Cricetinae Cercopithecus aethiops Mice, Inbred C57BL Drosophila melanogaster Mice, Knockout Drosophila

Diseases39

Genetic Predisposition to Disease Syndrome Alcoholism Genetic Diseases, X-Linked Colorectal Neoplasms, Hereditary Nonpolyposis Retinitis Pigmentosa Colorectal Neoplasms Abnormalities, Multiple Adenomatous Polyposis Coli Adenocarcinoma Hemochromatosis Chromosome Deletion Lung Neoplasms Eye Abnormalities Cardiomyopathy, Hypertrophic Cardiomyopathy, Hypertrophic, Familial Breast Neoplasms Disease Models, Animal Corneal Dystrophies, Hereditary Albinism, Oculocutaneous Ovarian Neoplasms Neoplastic Syndromes, Hereditary Cell Transformation, Neoplastic Hearing Loss, Sensorineural Familial Mediterranean Fever Adenoma Mitochondrial Diseases Deafness Multiple Endocrine Neoplasia Type 1 Cystic Fibrosis Hyperkeratosis, Epidermolytic Muscular Dystrophies Osteochondrodysplasias Eye Diseases, Hereditary Limb Deformities, Congenital Leukemia, Myeloid, Acute Paraganglioma Marfan Syndrome Craniofacial Abnormalities

Chemicals and Drugs63

Serotonin Plasma Membrane Transport Proteins Codon, Nonsense Codon DNA Primers DNA, Neoplasm DNA-Binding Proteins Membrane Proteins DNA Transcription Factors Nuclear Proteins Tumor Suppressor Protein p53 Proto-Oncogene Proteins B-raf Carrier Proteins Mutant Proteins DNA, Mitochondrial Mutagens Bacterial Proteins RNA, Messenger Proto-Oncogene Proteins Eye Proteins MutS Homolog 2 Protein Ethylnitrosourea Cytoskeletal Proteins Proteins ras Proteins Cystic Fibrosis Transmembrane Conductance Regulator RNA Splice Sites Hypoxanthine Phosphoribosyltransferase Neoplasm Proteins Genetic Markers Recombinant Proteins Adaptor Proteins, Signal Transducing DNA, Complementary Tumor Suppressor Proteins Trans-Activators Repressor Proteins Factor V Homeodomain Proteins Codon, Terminator Saccharomyces cerevisiae Proteins DNA, Bacterial BRCA1 Protein DNA Transposable Elements Recombinant Fusion Proteins Toll-Like Receptor 9 RNA, Transfer, Leu Ethyl Methanesulfonate Receptor, Epidermal Growth Factor Drosophila Proteins Escherichia coli Proteins Protein-Serine-Threonine Kinases Lamin Type A Fungal Proteins Nerve Tissue Proteins Adenosine Triphosphatases fms-Like Tyrosine Kinase 3 NAV1.5 Voltage-Gated Sodium Channel Von Hippel-Lindau Tumor Suppressor Protein Arginine Prothrombin Membrane Transport Proteins beta Catenin Connexins

Analytical, Diagnostic and Therapeutic Techniques and Equipment31

DNA Mutational Analysis Pedigree Polymerase Chain Reaction Models, Genetic Genetic Association Studies Amino Acid Substitution Genetic Testing Sequence Analysis, DNA Mutagenesis, Site-Directed Chromosome Mapping Heterozygote Detection Models, Molecular Risk Factors Genetic Complementation Test Sequence Alignment Cloning, Molecular Transfection Immunohistochemistry Mutagenesis, Insertional Reverse Transcriptase Polymerase Chain Reaction Crosses, Genetic Case-Control Studies Mutagenicity Tests Restriction Mapping Prognosis Disease Models, Animal Blotting, Western Cohort Studies Electroretinography Models, Biological Blotting, Southern

Psychiatry and Psychology4

Adult Children Life Change Events Alcoholism Family

Phenomena and Processes97

Point Mutation Mutation Mutation, Missense Gene-Environment Interaction Frameshift Mutation Genotype Germ-Line Mutation Phenotype Alleles Epistasis, Genetic Genetic Predisposition to Disease Polymorphism, Single-Stranded Conformational Heterozygote Exons Environment Base Sequence Polymorphism, Genetic Polymorphism, Single Nucleotide Genes, p53 Mutation Rate Amino Acid Substitution Codon, Nonsense Homozygote Amino Acid Sequence Genes, Recessive Sequence Deletion Codon Mutagenesis Genes, Dominant X Chromosome Gene Deletion Protein Structure, Tertiary Founder Effect Consanguinity Gene Frequency Genetic Linkage Genes, BRCA1 Sequence Homology, Amino Acid Suppression, Genetic Binding Sites Microsatellite Repeats Polymorphism, Restriction Fragment Length Genes, APC Penetrance Introns Exome Genes, ras Protein Binding Loss of Heterozygosity Transfection Genetic Variation Plasmids Mutagenesis, Insertional Genes, BRCA2 Promoter Regions, Genetic DNA Mismatch Repair Genes, Lethal Transcription, Genetic Signal Transduction Genes Genes, Bacterial RNA Splice Sites Recombination, Genetic Genetic Markers Kinetics Protein Conformation Gene Expression RNA Splicing DNA Repair Structure-Activity Relationship Base Pair Mismatch Chromosome Deletion INDEL Mutation Temperature Conserved Sequence Chromosomes, Human, Pair 17 Genetic Heterogeneity Drug Resistance, Viral Gene Expression Regulation, Neoplastic Gene Expression Regulation Mosaicism Drug Resistance Genes, Suppressor Genes, Tumor Suppressor Codon, Terminator Genes, Fungal DNA Transposable Elements Protein Structure, Secondary Time Factors Gene Amplification Drug Resistance, Microbial Selection, Genetic Evolution, Molecular Gene Dosage Alternative Splicing Phosphorylation Drug Resistance, Bacterial

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena3

Adult Children Social Environment Family

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Named Groups4

Adult Children Asian Continental Ancestry Group Jews Infant, Newborn

Health Care9

Environment Genetic Testing Family Health Risk Factors Age of Onset Case-Control Studies Temperature Cohort Studies Genetic Counseling

Geographicals3

China Italy Japan

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 Geographicals

Point Mutation Mutation Mutation, Missense Gene-Environment Interaction Frameshift Mutation Genotype DNA Mutational Analysis Germ-Line Mutation Pedigree Phenotype Alleles Epistasis, Genetic Genetic Predisposition to Disease Serotonin Plasma Membrane Transport Proteins Polymorphism, Single-Stranded Conformational Adult Children Heterozygote Exons Environment Polymerase Chain Reaction Base Sequence Models, Genetic Genetic Association Studies Polymorphism, Genetic Polymorphism, Single Nucleotide Molecular Sequence Data Genes, p53 Mutation Rate Amino Acid Substitution Genetic Testing Codon, Nonsense Homozygote Social Environment Sequence Analysis, DNA Amino Acid Sequence Life Change Events Genes, Recessive Mutagenesis, Site-Directed Sequence Deletion Codon Mutagenesis Genes, Dominant DNA Primers DNA, Neoplasm X Chromosome Syndrome Gene Deletion Alcoholism DNA-Binding Proteins Chromosome Mapping Membrane Proteins Protein Structure, Tertiary Founder Effect Family Health Heterozygote Detection Consanguinity Cell Line DNA Escherichia coli Models, Molecular Risk Factors Gene Frequency Genetic Linkage Transcription Factors Nuclear Proteins Tumor Suppressor Protein p53 Age of Onset Genes, BRCA1 Sequence Homology, Amino Acid Suppression, Genetic Proto-Oncogene Proteins B-raf Genetic Diseases, X-Linked Binding Sites Asian Continental Ancestry Group Genetic Complementation Test Microsatellite Repeats Carrier Proteins Polymorphism, Restriction Fragment Length Mutant Proteins Genes, APC Sequence Alignment Cloning, Molecular DNA, Mitochondrial Penetrance Introns Exome Genes, ras Mutagens Protein Binding Loss of Heterozygosity Bacterial Proteins Transfection Genetic Variation RNA, Messenger Proto-Oncogene Proteins Eye Proteins Plasmids Saccharomyces cerevisiae Colorectal Neoplasms, Hereditary Nonpolyposis Immunohistochemistry

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