Repeats polymorphism gene contains trinucleotide repeat expansion. Medical search. Frequent questions

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Anatomy3

Intranuclear Inclusion Bodies Cell Line Chromosomes, Human, X

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Mice, Transgenic Saccharomyces cerevisiae

Diseases20

Friedreich Ataxia Spinocerebellar Degenerations Myotonic Dystrophy Fragile X Syndrome Huntington Disease Genetic Predisposition to Disease Spinocerebellar Ataxias Machado-Joseph Disease Heredodegenerative Disorders, Nervous System Genomic Instability Frontotemporal Dementia Anticipation, Genetic Cerebellar Ataxia Chromosome Fragility Genetic Diseases, Inborn Muscular Dystrophy, Oculopharyngeal Amyotrophic Lateral Sclerosis Neurodegenerative Diseases Myoclonic Epilepsies, Progressive Disease Models, Animal

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Fragile X Mental Retardation Protein Iron-Binding Proteins Receptors, Androgen DNA Nerve Tissue Proteins Genetic Markers Flap Endonucleases Receptors, Dopamine D4 DNA Primers RNA-Binding Proteins DNA, Satellite Nuclear Proteins Proteins Peptides Aromatase 3-Oxo-5-alpha-Steroid 4-Dehydrogenase DNA-Binding Proteins RNA, Messenger MutS Homolog 2 Protein Nucleic Acid Heteroduplexes Interleukin 1 Receptor Antagonist Protein

Analytical, Diagnostic and Therapeutic Techniques and Equipment10

Polymerase Chain Reaction Pedigree Case-Control Studies Sequence Analysis, DNA Chromosome Mapping Models, Genetic DNA Mutational Analysis Disease Models, Animal Genetic Testing Cohort Studies

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes44

Trinucleotide Repeat Expansion Trinucleotide Repeats DNA Repeat Expansion Polymorphism, Genetic Alleles Dinucleotide Repeats Tandem Repeat Sequences Repetitive Sequences, Nucleic Acid Minisatellite Repeats Microsatellite Repeats Base Sequence Mutation Polymorphism, Single Nucleotide Genotype Gene Frequency Genetic Predisposition to Disease Haplotypes Genomic Instability Inverted Repeat Sequences Genetic Markers Genetic Variation Anticipation, Genetic Phenotype Nucleic Acid Conformation Genetic Linkage Exons Introns Chromosome Fragility Heterozygote Promoter Regions, Genetic DNA, Satellite Linkage Disequilibrium Repetitive Sequences, Amino Acid DNA Repair Amino Acid Sequence Genome, Human Transcription, Genetic Polymorphism, Restriction Fragment Length Ankyrin Repeat Genes, Dominant DNA Replication Recombination, Genetic Chromosomes, Human, X Sequence Deletion

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Base Sequence Molecular Sequence Data Amino Acid Sequence

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Asian Continental Ancestry Group European Continental Ancestry Group

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Case-Control Studies Age of Onset Genetic Testing Cohort Studies

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Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Information Science Named Groups Health Care Geographicals

Trinucleotide Repeat Expansion Trinucleotide Repeats Friedreich Ataxia DNA Repeat Expansion Spinocerebellar Degenerations Myotonic Dystrophy Fragile X Syndrome Polymorphism, Genetic Huntington Disease Fragile X Mental Retardation Protein Alleles Dinucleotide Repeats Tandem Repeat Sequences Iron-Binding Proteins Repetitive Sequences, Nucleic Acid Minisatellite Repeats Microsatellite Repeats Base Sequence Mutation Polymorphism, Single Nucleotide Genotype Gene Frequency Molecular Sequence Data Polymerase Chain Reaction Receptors, Androgen Genetic Predisposition to Disease Spinocerebellar Ataxias Machado-Joseph Disease Pedigree DNA Haplotypes Heredodegenerative Disorders, Nervous System Case-Control Studies Nerve Tissue Proteins Genomic Instability Sequence Analysis, DNA Inverted Repeat Sequences Genetic Markers Genetic Variation Frontotemporal Dementia Flap Endonucleases Anticipation, Genetic Phenotype Nucleic Acid Conformation Genetic Linkage Age of Onset Receptors, Dopamine D4 Exons Cerebellar Ataxia Chromosome Mapping Intranuclear Inclusion Bodies Introns Chromosome Fragility Heterozygote Genetic Diseases, Inborn Muscular Dystrophy, Oculopharyngeal DNA Primers RNA-Binding Proteins Promoter Regions, Genetic DNA, Satellite Nuclear Proteins Amyotrophic Lateral Sclerosis Linkage Disequilibrium Models, Genetic Repetitive Sequences, Amino Acid Neurodegenerative Diseases Proteins DNA Repair Peptides Asian Continental Ancestry Group Amino Acid Sequence Aromatase Genome, Human Mice, Transgenic Transcription, Genetic 3-Oxo-5-alpha-Steroid 4-Dehydrogenase DNA-Binding Proteins DNA Mutational Analysis Polymorphism, Restriction Fragment Length Ankyrin Repeat Genes, Dominant DNA Replication European Continental Ancestry Group RNA, Messenger Myoclonic Epilepsies, Progressive Saccharomyces cerevisiae MutS Homolog 2 Protein Nucleic Acid Heteroduplexes Interleukin 1 Receptor Antagonist Protein China Recombination, Genetic Cell Line Disease Models, Animal Genetic Testing Chromosomes, Human, X Sequence Deletion Cohort Studies

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