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

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Anatomy4

Intranuclear Inclusion Bodies Chromosomes, Human, X Cell Line Brain

Organisms2

Mice, Transgenic Saccharomyces cerevisiae

Diseases23

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 Genetic Diseases, Inborn Chromosome Fragility Muscular Dystrophy, Oculopharyngeal Amyotrophic Lateral Sclerosis Neurodegenerative Diseases Disease Models, Animal Myoclonic Epilepsies, Progressive Intellectual Disability

Chemicals and Drugs18

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment10

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

Psychiatry and Psychology3

Huntington Disease Frontotemporal Dementia Intellectual Disability

Phenomena and Processes38

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

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

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