Larger fmr1 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

Diseases20

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

Chemicals and Drugs16

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment5

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

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes30

Trinucleotide Repeat Expansion Trinucleotide Repeats DNA Repeat Expansion Alleles Mutation Repetitive Sequences, Nucleic Acid Base Sequence Genomic Instability Anticipation, Genetic Microsatellite Repeats Nucleic Acid Conformation Inverted Repeat Sequences Minisatellite Repeats Tandem Repeat Sequences Chromosome Fragility Polymorphism, Genetic Phenotype DNA Repair Genotype Heterozygote DNA Replication Genes, Dominant Transcription, Genetic Genome, Human Exons Genetic Markers Repetitive Sequences, Amino Acid Chromosomes, Human, X Amino Acid Sequence Gene Frequency

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Health Care1

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

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