Locus 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 Genetic Markers Receptors, Androgen Nuclear Proteins Nucleic Acid Heteroduplexes DNA Primers Peptides DNA, Satellite Oligodeoxyribonucleotides MutS Homolog 2 Protein DNA-Binding Proteins RNA, Messenger Saccharomyces cerevisiae Proteins Endodeoxyribonucleases RNA DNA, Fungal Proteins Transcription Factors Oligonucleotides DNA, Complementary Protein-Serine-Threonine Kinases

Analytical, Diagnostic and Therapeutic Techniques and Equipment11

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

Psychiatry and Psychology2

Huntington Disease Intellectual Disability

Phenomena and Processes44

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

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