Heterozygous trinucleotide repeats. Medical search. Frequent questions

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Anatomy4

Intranuclear Inclusion Bodies Chromosomes, Human, X X Chromosome Cell Line

Organisms2

Saccharomyces cerevisiae Mice, Transgenic

Diseases18

Friedreich Ataxia Fragile X Syndrome Myotonic Dystrophy Spinocerebellar Degenerations Huntington Disease Machado-Joseph Disease Heredodegenerative Disorders, Nervous System Genomic Instability Spinocerebellar Ataxias Anticipation, Genetic Chromosome Fragility Genetic Diseases, Inborn Cerebellar Ataxia Muscular Dystrophy, Oculopharyngeal Neurodegenerative Diseases Nervous System Diseases Intellectual Disability Disease Models, Animal

Chemicals and Drugs26

Fragile X Mental Retardation Protein DNA Nerve Tissue Proteins Flap Endonucleases Iron-Binding Proteins RNA-Binding Proteins Receptors, Androgen Nuclear Proteins Nucleic Acid Heteroduplexes Peptides DNA, Satellite DNA Primers Oligodeoxyribonucleotides Genetic Markers MutS Homolog 2 Protein Endodeoxyribonucleases Saccharomyces cerevisiae Proteins DNA-Binding Proteins RNA, Messenger RNA DNA, Fungal Proteins Oligonucleotides Protein-Serine-Threonine Kinases DNA, Complementary Transcription Factors

Analytical, Diagnostic and Therapeutic Techniques and Equipment10

Polymerase Chain Reaction Pedigree Sequence Analysis, DNA Models, Genetic Chromosome Mapping Nucleic Acid Denaturation Blotting, Southern Disease Models, Animal DNA Mutational Analysis Genetic Testing

Psychiatry and Psychology2

Huntington Disease Intellectual Disability

Phenomena and Processes42

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

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Health Care2

Age of Onset Genetic Testing

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

Trinucleotide Repeats Trinucleotide Repeat Expansion Friedreich Ataxia Fragile X Syndrome Myotonic Dystrophy Spinocerebellar Degenerations Huntington Disease Fragile X Mental Retardation Protein Repetitive Sequences, Nucleic Acid Base Sequence Machado-Joseph Disease Alleles Microsatellite Repeats Heredodegenerative Disorders, Nervous System Molecular Sequence Data Genomic Instability Nucleic Acid Conformation Minisatellite Repeats DNA Nerve Tissue Proteins Tandem Repeat Sequences Inverted Repeat Sequences Spinocerebellar Ataxias Flap Endonucleases Anticipation, Genetic Iron-Binding Proteins Chromosome Fragility Mutation Genetic Diseases, Inborn Polymerase Chain Reaction Polymorphism, Genetic Intranuclear Inclusion Bodies RNA-Binding Proteins Pedigree Cerebellar Ataxia Age of Onset Muscular Dystrophy, Oculopharyngeal Neurodegenerative Diseases Receptors, Androgen DNA Repair Nuclear Proteins Sequence Analysis, DNA Nucleic Acid Heteroduplexes Models, Genetic Peptides Chromosomes, Human, X Transcription, Genetic Dinucleotide Repeats DNA, Satellite DNA Replication Saccharomyces cerevisiae DNA Primers Phenotype Genome, Human Oligodeoxyribonucleotides Chromosome Mapping Genotype Genetic Markers MutS Homolog 2 Protein Amino Acid Sequence Nucleic Acid Denaturation Gene Frequency Sequence Deletion Exons Endodeoxyribonucleases Mice, Transgenic X Chromosome Nervous System Diseases Saccharomyces cerevisiae Proteins Heterozygote DNA-Binding Proteins Genes, Dominant RNA, Messenger Genetic Variation RNA Ankyrin Repeat Blotting, Southern Recombination, Genetic DNA, Fungal Cell Line Intellectual Disability Repetitive Sequences, Amino Acid Point Mutation Disease Models, Animal Proteins DNA Mutational Analysis Oligonucleotides Protein-Serine-Threonine Kinases Genetic Testing DNA, Complementary Promoter Regions, Genetic Genetic Linkage Transcription Factors Haplotypes Gene Expression

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