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

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Anatomy4

Intranuclear Inclusion Bodies Chromosomes, Human, X Brain Cell Line

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 Drugs16

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

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

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes31

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 Transcription, Genetic DNA Repair Genotype Chromosomes, Human, X Amino Acid Sequence Gene Frequency Exons Genes, Dominant DNA Replication Genome, Human Genetic Markers Repetitive Sequences, Amino Acid Mosaicism

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

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