Genetic premutation 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

Diseases22

Fragile X Syndrome Friedreich Ataxia Spinocerebellar Degenerations Myotonic Dystrophy Huntington Disease Ataxia Tremor Spinocerebellar Ataxias Machado-Joseph Disease Heredodegenerative Disorders, Nervous System Primary Ovarian Insufficiency Genomic Instability Frontotemporal Dementia Anticipation, Genetic Cerebellar Ataxia Chromosome Fragility Muscular Dystrophy, Oculopharyngeal Genetic Diseases, Inborn Amyotrophic Lateral Sclerosis Neurodegenerative Diseases Disease Models, Animal Myoclonic Epilepsies, Progressive

Chemicals and Drugs15

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

Pedigree Polymerase Chain Reaction Gene Knock-In Techniques Models, Genetic Genetic Testing Sequence Analysis, DNA Disease Models, Animal DNA Mutational Analysis Heterozygote Detection

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes30

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

Information Science2

Base Sequence Molecular Sequence Data

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 Fragile X Syndrome Fragile X Mental Retardation Protein Friedreich Ataxia DNA Repeat Expansion Spinocerebellar Degenerations Myotonic Dystrophy Huntington Disease Iron-Binding Proteins Alleles Ataxia Mutation Tremor Repetitive Sequences, Nucleic Acid Spinocerebellar Ataxias Machado-Joseph Disease Nerve Tissue Proteins Base Sequence Intranuclear Inclusion Bodies Heredodegenerative Disorders, Nervous System Primary Ovarian Insufficiency Heterozygote Pedigree Genomic Instability Molecular Sequence Data DNA Frontotemporal Dementia Flap Endonucleases Anticipation, Genetic Microsatellite Repeats RNA-Binding Proteins Nucleic Acid Conformation Age of Onset Inverted Repeat Sequences Minisatellite Repeats Tandem Repeat Sequences Cerebellar Ataxia Polymerase Chain Reaction Chromosome Fragility Muscular Dystrophy, Oculopharyngeal Genetic Diseases, Inborn Phenotype Amyotrophic Lateral Sclerosis Polymorphism, Genetic Neurodegenerative Diseases Nuclear Proteins Gene Knock-In Techniques Models, Genetic Peptides Proteins DNA Repair Mice, Transgenic Genetic Testing Genotype Sequence Analysis, DNA Receptors, Androgen RNA, Messenger Disease Models, Animal Chromosomes, Human, X Gene Frequency Transcription, Genetic DNA Primers Genes, Dominant Myoclonic Epilepsies, Progressive DNA Replication DNA Mutational Analysis Genome, Human Heterozygote Detection MutS Homolog 2 Protein Genetic Markers Repetitive Sequences, Amino Acid Exons Nucleic Acid Heteroduplexes Saccharomyces cerevisiae Mosaicism

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