Polymorphism trinucleotide. Medical search. Frequent questions

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

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Saccharomyces cerevisiae Mice, Transgenic Escherichia coli

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Genetic Predisposition to Disease Friedreich Ataxia Fragile X Syndrome Huntington Disease Spinocerebellar Degenerations Machado-Joseph Disease Heredodegenerative Disorders, Nervous System Genomic Instability Genetic Diseases, Inborn Muscular Dystrophy, Oculopharyngeal Chromosome Fragility Anticipation, Genetic Cerebellar Ataxia Neurodegenerative Diseases Muscular Atrophy, Spinal Ataxia Nervous System Diseases Disease Models, Animal Intellectual Disability Diabetes Mellitus, Type 2 Colorectal Neoplasms Breast Neoplasms Disease Susceptibility

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Fragile X Mental Retardation Protein DNA Genetic Markers DNA Primers Nerve Tissue Proteins Oligonucleotides Codon Flap Endonucleases Iron-Binding Proteins RNA-Binding Proteins Methylenetetrahydrofolate Reductase (NADPH2)Receptors, Androgen Oligodeoxyribonucleotides Nucleic Acid Heteroduplexes Nucleotides Nuclear Proteins Guanine Peptides RNA, Messenger DNA-Binding Proteins DNA, Plant Peptidyl-Dipeptidase A Glutathione Transferase Catechol O-Methyltransferase RNA Cytosine DNA, Satellite Glutathione S-Transferase pi Oligoribonucleotides Polydeoxyribonucleotides DNA, Bacterial Deoxyribonucleases, Type II Site-Specific Proteins DNA, Fungal Serotonin Plasma Membrane Transport Proteins Transcription Factors Xeroderma Pigmentosum Group D Protein DNA, Complementary Aryl Hydrocarbon Hydroxylases MutS Homolog 2 Protein Adenine Saccharomyces cerevisiae Proteins Endodeoxyribonucleases Receptors, Calcitriol Aryldialkylphosphatase DNA, Single-Stranded Arylamine N-Acetyltransferase Cytochrome P-450 CYP1A1 Protein-Serine-Threonine Kinases RNA, Transfer 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase DNA Helicases Valine Cytochrome P-450 CYP2E1 3' Untranslated Regions Bacterial Proteins Glucuronosyltransferase Apolipoproteins E RNA, Bacterial DNA, Mitochondrial Mannose-Binding Lectin

Analytical, Diagnostic and Therapeutic Techniques and Equipment32

Polymerase Chain Reaction Case-Control Studies Sequence Analysis, DNA Genetic Association Studies Pedigree Models, Genetic Chromosome Mapping DNA Mutational Analysis Risk Factors Amplified Fragment Length Polymorphism Analysis Genetic Testing Odds Ratio Genome-Wide Association Study Gene Knock-In Techniques Amino Acid Substitution Blotting, Southern Cloning, Molecular Cohort Studies Nucleic Acid Denaturation Models, Molecular Risk Sequence Alignment Genotyping Techniques DNA Fingerprinting Disease Models, Animal Logistic Models Chi-Square Distribution Heterozygote Detection Circular Dichroism Bacterial Typing Techniques Magnetic Resonance Spectroscopy Transfection

Psychiatry and Psychology4

Huntington Disease Fathers Smoking Intellectual Disability

Phenomena and Processes96

Trinucleotide Repeats Trinucleotide Repeat Expansion Polymorphism, Genetic Polymorphism, Single Nucleotide Alleles Gene Frequency Genetic Predisposition to Disease Base Sequence Haplotypes Genotype Microsatellite Repeats Repetitive Sequences, Nucleic Acid Genetic Variation Nucleic Acid Conformation Polymorphism, Single-Stranded Conformational Mutation Genetic Markers Linkage Disequilibrium Phenotype Minisatellite Repeats Heterozygote Genomic Instability Exons Promoter Regions, Genetic Dinucleotide Repeats Codon Tandem Repeat Sequences Homozygote Genetic Linkage Chromosome Fragility Genome, Human DNA Repair Anticipation, Genetic Point Mutation Introns Genetic Loci Amino Acid Sequence Inverted Repeat Sequences Phylogeny Transcription, Genetic Chromosome Fragile Sites Odds Ratio Evolution, Molecular Sequence Deletion Expressed Sequence Tags Sequence Tagged Sites Species Specificity Chromosomes, Human, X Amino Acid Substitution X Chromosome Mosaicism Recombination, Genetic Genes, Dominant DNA, Satellite DNA Replication Nucleic Acid Denaturation Genome, Plant Sequence Homology, Nucleic Acid Binding Sites INDEL Mutation Base Pairing Risk Selection, Genetic Mutagenesis Templates, Genetic Gene Expression Base Composition Base Pair Mismatch Genes DNA, Single-Stranded Mutation, Missense Open Reading Frames Genome, Fungal Conserved Sequence Consensus Sequence Gene Expression Regulation Chi-Square Distribution Quantitative Trait Loci Kinetics Sequence Homology, Amino Acid DNA Methylation 3' Untranslated Regions Epistasis, Genetic DNA Damage Thermodynamics Plasmids Protein Binding Substrate Specificity Regulatory Sequences, Nucleic Acid Gene Deletion Gene-Environment Interaction RNA Splicing Genes, p53 Disease Susceptibility Protein Biosynthesis Transfection

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Genetics, Population Pharmacogenetics

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Fathers DNA Fingerprinting

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Base Sequence Molecular Sequence Data Amino Acid Sequence Phylogeny Publication Bias

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Trinucleotide Repeats Trinucleotide Repeat Expansion Polymorphism, Genetic Polymorphism, Single Nucleotide Alleles Gene Frequency Genetic Predisposition to Disease Friedreich Ataxia Base Sequence Fragile X Syndrome Huntington Disease Polymerase Chain Reaction Haplotypes Spinocerebellar Degenerations Molecular Sequence Data Genotype Case-Control Studies Fragile X Mental Retardation Protein Microsatellite Repeats Repetitive Sequences, Nucleic Acid Genetic Variation DNA Sequence Analysis, DNA Nucleic Acid Conformation Machado-Joseph Disease Polymorphism, Single-Stranded Conformational Mutation Genetic Association Studies Genetic Markers Linkage Disequilibrium Asian Continental Ancestry Group Phenotype Minisatellite Repeats DNA Primers Pedigree Heterozygote Nerve Tissue Proteins Heredodegenerative Disorders, Nervous System Models, Genetic Genomic Instability Exons Chromosome Mapping Age of Onset Promoter Regions, Genetic Oligonucleotides Dinucleotide Repeats DNA Mutational Analysis Codon Tandem Repeat Sequences Homozygote Risk Factors Genetic Linkage Flap Endonucleases Genetic Diseases, Inborn Iron-Binding Proteins Muscular Dystrophy, Oculopharyngeal Chromosome Fragility Genetics, Population Genome, Human RNA-Binding Proteins Methylenetetrahydrofolate Reductase (NADPH2)DNA Repair European Continental Ancestry Group Amplified Fragment Length Polymorphism Analysis Anticipation, Genetic Receptors, Androgen China Cerebellar Ataxia Point Mutation Oligodeoxyribonucleotides Introns Genetic Loci Amino Acid Sequence Inverted Repeat Sequences Nucleic Acid Heteroduplexes Nucleotides Nuclear Proteins Phylogeny Genetic Testing Guanine Peptides Transcription, Genetic Intranuclear Inclusion Bodies Chromosome Fragile Sites RNA, Messenger Odds Ratio DNA-Binding Proteins Evolution, Molecular DNA, Plant Neurodegenerative Diseases Genome-Wide Association Study Sequence Deletion Expressed Sequence Tags Sequence Tagged Sites Species Specificity Peptidyl-Dipeptidase A Chromosomes, Human, X Glutathione Transferase Catechol O-Methyltransferase Gene Knock-In Techniques

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