Triplet premutation gene contains trinucleotide repeat expansion. Medical search. Frequent questions

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Anatomy3

Intranuclear Inclusion Bodies Chromosomes, Human, X Brain

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 Anticipation, Genetic Frontotemporal Dementia Cerebellar Ataxia Muscular Dystrophy, Oculopharyngeal Chromosome Fragility Genetic Diseases, Inborn Amyotrophic Lateral Sclerosis Neurodegenerative Diseases Disease Models, Animal Myoclonic Epilepsies, Progressive

Chemicals and Drugs16

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

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

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes32

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

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Named Groups1

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

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