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

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Anatomy3

Intranuclear Inclusion Bodies Chromosomes, Human, X Cell Line

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 Drugs20

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

Pedigree Polymerase Chain Reaction Sequence Analysis, DNA Chromosome Mapping Models, Genetic DNA Mutational Analysis Cloning, Molecular Genetic Testing 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 Microsatellite Repeats Nucleic Acid Conformation Genomic Instability Anticipation, Genetic Inverted Repeat Sequences Minisatellite Repeats Tandem Repeat Sequences Phenotype Chromosome Fragility Polymorphism, Genetic Amino Acid Sequence Genetic Markers Genome, Human Genotype Genetic Linkage DNA Repair Genes, Dominant Haplotypes Polymorphism, Single Nucleotide Exons Transcription, Genetic Genetic Variation Gene Frequency Heterozygote DNA Replication Repetitive Sequences, Amino Acid Genetic Predisposition to Disease Chromosomes, Human, X Recombination, Genetic DNA, Satellite Sequence Deletion

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

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