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

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Anatomy4

Intranuclear Inclusion Bodies Chromosomes, Human, X Cell Line X Chromosome

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 Disease Neurodegenerative Diseases Disease Models, Animal Myoclonic Epilepsies, Progressive Genetic Predisposition to Disease

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 DNA Primers Receptors, Androgen RNA, Messenger DNA-Binding Proteins DNA, Satellite MutS Homolog 2 Protein Nucleic Acid Heteroduplexes

Analytical, Diagnostic and Therapeutic Techniques and Equipment8

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

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes45

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

Information Science4

Base Sequence Molecular Sequence Data Amino Acid Sequence Phylogeny

Health Care2

Age of Onset Genetic Testing

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

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