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

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Anatomy4

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

Organisms2

Mice, Transgenic Saccharomyces cerevisiae

Diseases20

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 Genetic Predisposition to Disease Cerebellar Ataxia Chromosome Fragility Muscular Dystrophy, Oculopharyngeal Genetic Diseases, Inborn Amyotrophic Lateral Sclerosis Neurodegenerative Diseases Myoclonic Epilepsies, Progressive Disease Models, Animal

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment13

Polymerase Chain Reaction Amplified Fragment Length Polymorphism Analysis Pedigree Sequence Analysis, DNA Case-Control Studies Models, Genetic Chromosome Mapping DNA Fingerprinting DNA Mutational Analysis Blotting, Southern Bacterial Typing Techniques Genetic Testing Disease Models, Animal

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes44

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

Anthropology, Education, Sociology and Social Phenomena1

DNA Fingerprinting

Information Science4

Base Sequence Molecular Sequence Data Phylogeny Amino Acid Sequence

Named Groups1

Asian Continental Ancestry Group

Health Care3

Age of Onset Case-Control Studies Genetic Testing

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups 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 Polymorphism, Restriction Fragment Length Iron-Binding Proteins Alleles Polymorphism, Genetic Mutation Repetitive Sequences, Nucleic Acid Base Sequence Polymorphism, Single Nucleotide Polymerase Chain Reaction Molecular Sequence Data Spinocerebellar Ataxias Amplified Fragment Length Polymorphism Analysis Machado-Joseph Disease Heredodegenerative Disorders, Nervous System Genotype DNA Microsatellite Repeats Gene Frequency Minisatellite Repeats Nerve Tissue Proteins Genomic Instability Pedigree Sequence Analysis, DNA Frontotemporal Dementia Flap Endonucleases Tandem Repeat Sequences Anticipation, Genetic Nucleic Acid Conformation Age of Onset Inverted Repeat Sequences Genetic Predisposition to Disease Genetic Variation Genetic Markers Haplotypes Phenotype Cerebellar Ataxia Intranuclear Inclusion Bodies Chromosome Fragility Muscular Dystrophy, Oculopharyngeal Genetic Diseases, Inborn DNA Primers RNA-Binding Proteins Case-Control Studies Heterozygote Models, Genetic Amyotrophic Lateral Sclerosis Chromosome Mapping Nuclear Proteins DNA Fingerprinting Neurodegenerative Diseases Exons DNA Repair Proteins Genetic Linkage Peptides Phylogeny Receptors, Androgen DNA, Bacterial Amino Acid Sequence DNA Mutational Analysis Genome, Human Genes, Dominant Mice, Transgenic Transcription, Genetic DNA-Binding Proteins RNA, Messenger Blotting, Southern Bacterial Typing Techniques Promoter Regions, Genetic Dinucleotide Repeats DNA Replication Myoclonic Epilepsies, Progressive Recombination, Genetic Repetitive Sequences, Amino Acid MutS Homolog 2 Protein Saccharomyces cerevisiae Nucleic Acid Heteroduplexes Asian Continental Ancestry Group DNA, Satellite DNA, Fungal Genetic Testing Disease Models, Animal X Chromosome Cell Line DNA, Ribosomal Chromosomes, Human, X Point Mutation Species Specificity

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