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

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Anatomy3

Intranuclear Inclusion Bodies Chromosomes, Human, X 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 Genetic Predisposition to Disease Disease Models, Animal Myoclonic Epilepsies, Progressive

Chemicals and Drugs17

Fragile X Mental Retardation Protein Iron-Binding Proteins Nerve Tissue Proteins DNA Flap Endonucleases Genetic Markers RNA-Binding Proteins 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 Chromosome Mapping Polymerase Chain Reaction Models, Genetic Sequence Analysis, DNA DNA Mutational Analysis Genetic Testing Disease Models, Animal

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes39

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

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

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