Protein trinucleotide. Medical search. Frequent questions

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Anatomy4

Intranuclear Inclusion Bodies Chromosomes, Human, X X Chromosome Cell Line

Organisms3

Saccharomyces cerevisiae Mice, Transgenic Escherichia coli

Diseases18

Friedreich Ataxia Fragile X Syndrome Huntington Disease Spinocerebellar Degenerations Machado-Joseph Disease Heredodegenerative Disorders, Nervous System Genomic Instability Muscular Dystrophy, Oculopharyngeal Chromosome Fragility Anticipation, Genetic Cerebellar Ataxia Genetic Diseases, Inborn Neurodegenerative Diseases Muscular Atrophy, Spinal Ataxia Nervous System Diseases Disease Models, Animal Intellectual Disability

Chemicals and Drugs36

Fragile X Mental Retardation Protein DNA Nerve Tissue Proteins Oligonucleotides Flap Endonucleases Iron-Binding Proteins RNA-Binding Proteins Receptors, Androgen Oligodeoxyribonucleotides Nucleic Acid Heteroduplexes Nucleotides Peptides DNA Primers Nuclear Proteins Guanine RNA Oligoribonucleotides Polydeoxyribonucleotides Codon RNA, Messenger Genetic Markers DNA, Satellite MutS Homolog 2 Protein DNA-Binding Proteins Saccharomyces cerevisiae Proteins Endodeoxyribonucleases DNA, Plant Cytosine DNA, Fungal DNA, Single-Stranded RNA, Transfer Adenine DNA, Complementary Proteins Transcription Factors Protein-Serine-Threonine Kinases

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

Polymerase Chain Reaction Pedigree Sequence Analysis, DNA Models, Genetic Gene Knock-In Techniques Chromosome Mapping Nucleic Acid Denaturation Models, Molecular DNA Mutational Analysis Blotting, Southern Disease Models, Animal Cloning, Molecular Genetic Testing Circular Dichroism Magnetic Resonance Spectroscopy

Psychiatry and Psychology3

Huntington Disease Fathers Intellectual Disability

Phenomena and Processes56

Trinucleotide Repeats Trinucleotide Repeat Expansion Base Sequence Repetitive Sequences, Nucleic Acid Nucleic Acid Conformation Alleles Microsatellite Repeats Genomic Instability Chromosome Fragility Mutation Polymorphism, Genetic Anticipation, Genetic Minisatellite Repeats Inverted Repeat Sequences Chromosome Fragile Sites Dinucleotide Repeats DNA Repair Tandem Repeat Sequences Transcription, Genetic Mosaicism Genetic Variation Chromosomes, Human, X Codon Sequence Tagged Sites Genotype Phenotype DNA Replication Genome, Human Genetic Markers Heterozygote Gene Frequency Expressed Sequence Tags Exons DNA, Satellite Amino Acid Sequence Templates, Genetic Point Mutation Sequence Deletion Nucleic Acid Denaturation Base Pairing Mutagenesis Genes, Dominant X Chromosome Binding Sites Genetic Loci DNA, Single-Stranded Recombination, Genetic Base Composition Genome, Fungal Base Pair Mismatch Promoter Regions, Genetic Consensus Sequence Kinetics Genetic Linkage Thermodynamics Evolution, Molecular

Anthropology, Education, Sociology and Social Phenomena1

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 Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care

Trinucleotide Repeats Trinucleotide Repeat Expansion Friedreich Ataxia Fragile X Syndrome Huntington Disease Spinocerebellar Degenerations Fragile X Mental Retardation Protein Base Sequence Repetitive Sequences, Nucleic Acid Nucleic Acid Conformation Machado-Joseph Disease Alleles Molecular Sequence Data Microsatellite Repeats DNA Heredodegenerative Disorders, Nervous System Genomic Instability Nerve Tissue Proteins Oligonucleotides Flap Endonucleases Muscular Dystrophy, Oculopharyngeal Chromosome Fragility Iron-Binding Proteins Mutation Polymerase Chain Reaction Polymorphism, Genetic RNA-Binding Proteins Anticipation, Genetic Cerebellar Ataxia Pedigree Genetic Diseases, Inborn Minisatellite Repeats Inverted Repeat Sequences Age of Onset Receptors, Androgen Oligodeoxyribonucleotides Nucleic Acid Heteroduplexes Intranuclear Inclusion Bodies Nucleotides Chromosome Fragile Sites Dinucleotide Repeats Sequence Analysis, DNA Neurodegenerative Diseases Peptides Models, Genetic DNA Repair Tandem Repeat Sequences DNA Primers Nuclear Proteins Gene Knock-In Techniques Guanine Transcription, Genetic RNA Oligoribonucleotides Mosaicism Genetic Variation Polydeoxyribonucleotides Chromosomes, Human, X Codon Sequence Tagged Sites Genotype Phenotype DNA Replication Saccharomyces cerevisiae Genome, Human RNA, Messenger Genetic Markers Chromosome Mapping Heterozygote Muscular Atrophy, Spinal Gene Frequency Expressed Sequence Tags Exons DNA, Satellite Amino Acid Sequence Mice, Transgenic Ataxia Templates, Genetic Point Mutation Sequence Deletion Nucleic Acid Denaturation Models, Molecular MutS Homolog 2 Protein Base Pairing Mutagenesis Genes, Dominant DNA-Binding Proteins X Chromosome Nervous System Diseases Saccharomyces cerevisiae Proteins Escherichia coli Endodeoxyribonucleases Fathers DNA Mutational Analysis Binding Sites DNA, Plant Cytosine Genetic Loci Blotting, Southern DNA, Fungal

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