Exon microsatellites gene contains trinucleotide repeat expansion. Medical search. Frequent questions

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Anatomy2

Intranuclear Inclusion Bodies Chromosomes, Human, X

Organisms2

Mice, Transgenic Saccharomyces cerevisiae

Diseases19

Friedreich Ataxia Spinocerebellar Degenerations Myotonic Dystrophy Fragile X Syndrome Huntington 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

Chemicals and Drugs18

Fragile X Mental Retardation Protein Iron-Binding Proteins Nerve Tissue Proteins DNA Genetic Markers Flap Endonucleases DNA, Satellite RNA-Binding Proteins DNA Primers Nuclear Proteins Proteins Peptides Receptors, Androgen MutS Homolog 2 Protein RNA, Messenger DNA, Plant DNA-Binding Proteins Nucleic Acid Heteroduplexes

Analytical, Diagnostic and Therapeutic Techniques and Equipment7

Pedigree Polymerase Chain Reaction Sequence Analysis, DNA Models, Genetic Chromosome Mapping DNA Mutational Analysis Disease Models, Animal

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes42

Trinucleotide Repeat Expansion Trinucleotide Repeats DNA Repeat Expansion Exons Microsatellite Repeats Alleles Mutation Repetitive Sequences, Nucleic Acid Base Sequence Polymorphism, Genetic Genomic Instability Dinucleotide Repeats Genetic Markers Minisatellite Repeats Anticipation, Genetic Tandem Repeat Sequences Nucleic Acid Conformation Genetic Variation Inverted Repeat Sequences DNA, Satellite Chromosome Fragility Genotype Phenotype Haplotypes Heterozygote Gene Frequency Genome, Human DNA Repair Genetic Linkage Evolution, Molecular Transcription, Genetic Amino Acid Sequence Genes, Dominant DNA Replication Expressed Sequence Tags Introns Recombination, Genetic Chromosomes, Human, X Repetitive Sequences, Amino Acid Genetic Loci Phylogeny Sequence Deletion

Disciplines and Occupations1

Genetics, Population

Information Science4

Base Sequence Molecular Sequence Data Amino Acid Sequence Phylogeny

Health Care1

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

Trinucleotide Repeat Expansion Trinucleotide Repeats Friedreich Ataxia DNA Repeat Expansion Spinocerebellar Degenerations Myotonic Dystrophy Fragile X Syndrome Huntington Disease Fragile X Mental Retardation Protein Exons Microsatellite Repeats Iron-Binding Proteins Alleles Mutation Repetitive Sequences, Nucleic Acid Base Sequence Spinocerebellar Ataxias Machado-Joseph Disease Molecular Sequence Data Heredodegenerative Disorders, Nervous System Nerve Tissue Proteins DNA Polymorphism, Genetic Genomic Instability Dinucleotide Repeats Pedigree Genetic Markers Polymerase Chain Reaction Minisatellite Repeats Frontotemporal Dementia Flap Endonucleases Anticipation, Genetic Tandem Repeat Sequences Nucleic Acid Conformation Genetic Variation Inverted Repeat Sequences DNA, Satellite Sequence Analysis, DNA Cerebellar Ataxia Age of Onset Intranuclear Inclusion Bodies Chromosome Fragility Genetic Diseases, Inborn Muscular Dystrophy, Oculopharyngeal Genotype Models, Genetic RNA-Binding Proteins DNA Primers Chromosome Mapping Phenotype Amyotrophic Lateral Sclerosis Haplotypes Heterozygote Gene Frequency Nuclear Proteins Neurodegenerative Diseases Genetics, Population Genome, Human DNA Repair Genetic Linkage Proteins Peptides Receptors, Androgen Mice, Transgenic Evolution, Molecular Transcription, Genetic Amino Acid Sequence Genes, Dominant MutS Homolog 2 Protein DNA Mutational Analysis RNA, Messenger DNA, Plant DNA Replication Expressed Sequence Tags Introns DNA-Binding Proteins Saccharomyces cerevisiae Myoclonic Epilepsies, Progressive Recombination, Genetic Chromosomes, Human, X Repetitive Sequences, Amino Acid Nucleic Acid Heteroduplexes Genetic Loci Phylogeny Sequence Deletion Disease Models, Animal

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