Triplet repeat fmr1 gene contains trinucleotide repeat expansion. Medical search. Frequent questions

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Anatomy3

Intranuclear Inclusion Bodies Cell Line Chromosomes, Human, X

Organisms2

Saccharomyces cerevisiae Mice, Transgenic

Diseases21

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

Chemicals and Drugs18

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment6

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

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes37

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

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

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Health Care1

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

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

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