Inheritance 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 Anticipation, Genetic Frontotemporal Dementia Cerebellar Ataxia Genetic Diseases, Inborn Chromosome Fragility Muscular Dystrophy, Oculopharyngeal Amyotrophic Lateral Sclerosis Neurodegenerative Diseases Ataxia Disease Models, Animal Myoclonic Epilepsies, Progressive

Chemicals and Drugs17

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment7

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

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes34

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

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

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