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

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Anatomy2

Intranuclear Inclusion Bodies Chromosomes, Human, X

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 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 Models, Genetic Chromosome Mapping Sequence Analysis, DNA DNA Mutational Analysis Disease Models, Animal Genetic Testing

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

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

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