Stable trinucleotide repeats. Medical search. Frequent questions

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Anatomy5

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

Organisms2

Saccharomyces cerevisiae Mice, Transgenic

Diseases18

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

Chemicals and Drugs26

Fragile X Mental Retardation Protein DNA Nerve Tissue Proteins Flap Endonucleases Iron-Binding Proteins RNA-Binding Proteins Receptors, Androgen Nuclear Proteins Nucleic Acid Heteroduplexes Peptides DNA Primers DNA, Satellite Oligodeoxyribonucleotides Genetic Markers MutS Homolog 2 Protein Saccharomyces cerevisiae Proteins Endodeoxyribonucleases RNA, Messenger DNA-Binding Proteins RNA DNA, Fungal Proteins Oligonucleotides Protein-Serine-Threonine Kinases DNA, Complementary Transcription Factors

Analytical, Diagnostic and Therapeutic Techniques and Equipment10

Polymerase Chain Reaction Pedigree Sequence Analysis, DNA Models, Genetic Chromosome Mapping Nucleic Acid Denaturation Blotting, Southern Disease Models, Animal DNA Mutational Analysis Genetic Testing

Psychiatry and Psychology2

Huntington Disease Intellectual Disability

Phenomena and Processes42

Trinucleotide Repeats Trinucleotide Repeat Expansion Repetitive Sequences, Nucleic Acid Base Sequence Alleles Microsatellite Repeats Nucleic Acid Conformation Genomic Instability Minisatellite Repeats Tandem Repeat Sequences Inverted Repeat Sequences Anticipation, Genetic Chromosome Fragility Mutation Polymorphism, Genetic DNA Repair Transcription, Genetic Chromosomes, Human, X DNA Replication Phenotype DNA, Satellite Dinucleotide Repeats Amino Acid Sequence Genome, Human Genotype Genetic Markers Nucleic Acid Denaturation Sequence Deletion Gene Frequency Exons X Chromosome Heterozygote Genes, Dominant Genetic Variation Recombination, Genetic Ankyrin Repeat Point Mutation Repetitive Sequences, Amino Acid Promoter Regions, Genetic Gene Expression Genetic Linkage Haplotypes

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 Repeats Trinucleotide Repeat Expansion Friedreich Ataxia Fragile X Syndrome Myotonic Dystrophy Spinocerebellar Degenerations Huntington Disease Fragile X Mental Retardation Protein Repetitive Sequences, Nucleic Acid Base Sequence Machado-Joseph Disease Alleles Molecular Sequence Data Microsatellite Repeats Heredodegenerative Disorders, Nervous System Nucleic Acid Conformation Genomic Instability DNA Minisatellite Repeats Nerve Tissue Proteins Tandem Repeat Sequences Inverted Repeat Sequences Spinocerebellar Ataxias Flap Endonucleases Anticipation, Genetic Iron-Binding Proteins Chromosome Fragility Mutation Polymerase Chain Reaction Genetic Diseases, Inborn Polymorphism, Genetic RNA-Binding Proteins Intranuclear Inclusion Bodies Pedigree Cerebellar Ataxia Age of Onset Muscular Dystrophy, Oculopharyngeal Neurodegenerative Diseases Receptors, Androgen DNA Repair Nuclear Proteins Sequence Analysis, DNA Nucleic Acid Heteroduplexes Models, Genetic Peptides Transcription, Genetic Chromosomes, Human, X DNA Replication Saccharomyces cerevisiae DNA Primers Phenotype DNA, Satellite Dinucleotide Repeats Amino Acid Sequence Genome, Human Oligodeoxyribonucleotides Chromosome Mapping Genotype Genetic Markers Nucleic Acid Denaturation MutS Homolog 2 Protein Sequence Deletion Gene Frequency Mice, Transgenic Saccharomyces cerevisiae Proteins Exons Endodeoxyribonucleases RNA, Messenger X Chromosome Nervous System Diseases DNA-Binding Proteins Heterozygote Genes, Dominant Genetic Variation Cell Line RNA Recombination, Genetic Blotting, Southern Ankyrin Repeat DNA, Fungal Proteins Point Mutation Intellectual Disability Disease Models, Animal Repetitive Sequences, Amino Acid Oligonucleotides DNA Mutational Analysis Protein-Serine-Threonine Kinases Promoter Regions, Genetic Genetic Testing DNA, Complementary Transcription Factors Gene Expression Genetic Linkage Haplotypes Brain

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