Intron 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 Drugs27

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment12

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

Psychiatry and Psychology2

Huntington Disease Intellectual Disability

Phenomena and Processes49

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

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

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