Phenotype abnormal gene contains trinucleotide repeat expansion. Medical search. Frequent questions

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Anatomy2

Intranuclear Inclusion Bodies Cell Line

Organisms2

Mice, Transgenic Saccharomyces cerevisiae

Diseases19

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

Chemicals and Drugs17

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 RNA, Messenger Genetic Markers DNA-Binding Proteins MutS Homolog 2 Protein Nucleic Acid Heteroduplexes Saccharomyces cerevisiae Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment7

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

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes30

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

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

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