Genetic 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 Disease Amyotrophic Lateral Sclerosis Neurodegenerative Diseases 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 Proteins Nuclear Proteins Peptides DNA Primers Receptors, Androgen 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 Models, Genetic Chromosome Mapping Sequence Analysis, DNA Genetic Testing DNA Mutational Analysis Disease Models, Animal

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes38

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

Disciplines and Occupations1

Genetics, Medical

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

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