Disorders diseases gene contains trinucleotide repeat expansion. Medical search. Frequent questions

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Anatomy3

Intranuclear Inclusion Bodies Chromosomes, Human, X Brain

Organisms2

Mice, Transgenic Saccharomyces cerevisiae

Diseases21

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

Chemicals and Drugs17

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment8

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

Psychiatry and Psychology4

Huntington Disease Frontotemporal Dementia Bipolar Disorder Mental Disorders

Phenomena and Processes35

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

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Health Care2

Age of Onset Genetic Testing

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

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