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

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Anatomy3

Intranuclear Inclusion Bodies Chromosomes, Human, X Cell Line

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 Drugs17

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

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 Processes34

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

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Health Care1

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

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

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