Intronic polymorphism gene contains trinucleotide repeat expansion. Medical search. Frequent questions

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Anatomy3

Intranuclear Inclusion Bodies Cell Line Chromosomes, Human, X

Organisms2

Mice, Transgenic Saccharomyces cerevisiae

Diseases20

Friedreich Ataxia Spinocerebellar Degenerations Myotonic Dystrophy Fragile X Syndrome Huntington Disease Spinocerebellar Ataxias Machado-Joseph Disease Heredodegenerative Disorders, Nervous System Genomic Instability Frontotemporal Dementia Anticipation, Genetic Cerebellar Ataxia Genetic Predisposition to Disease Chromosome Fragility Muscular Dystrophy, Oculopharyngeal Genetic Diseases, Inborn Amyotrophic Lateral Sclerosis Neurodegenerative Diseases Myoclonic Epilepsies, Progressive Disease Models, Animal

Chemicals and Drugs16

Fragile X Mental Retardation Protein Iron-Binding Proteins Nerve Tissue Proteins DNA Flap Endonucleases RNA-Binding Proteins Nuclear Proteins DNA Primers Genetic Markers Proteins Peptides Receptors, Androgen RNA, Messenger DNA-Binding Proteins MutS Homolog 2 Protein Nucleic Acid Heteroduplexes

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

Polymerase Chain Reaction Pedigree Sequence Analysis, DNA Models, Genetic Case-Control Studies DNA Mutational Analysis Chromosome Mapping Genetic Testing Disease Models, Animal

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes40

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

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Health Care3

Age of Onset Case-Control Studies 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 Repeat Expansion Trinucleotide Repeats Friedreich Ataxia DNA Repeat Expansion Introns Spinocerebellar Degenerations Myotonic Dystrophy Fragile X Syndrome Polymorphism, Genetic Huntington Disease Fragile X Mental Retardation Protein Alleles Polymorphism, Single Nucleotide Iron-Binding Proteins Genotype Mutation Repetitive Sequences, Nucleic Acid Base Sequence Spinocerebellar Ataxias Machado-Joseph Disease Molecular Sequence Data Heredodegenerative Disorders, Nervous System Nerve Tissue Proteins Microsatellite Repeats DNA Polymerase Chain Reaction Genomic Instability Pedigree Frontotemporal Dementia Minisatellite Repeats Flap Endonucleases Gene Frequency Anticipation, Genetic Nucleic Acid Conformation Tandem Repeat Sequences Age of Onset Inverted Repeat Sequences Exons Cerebellar Ataxia Genetic Predisposition to Disease RNA-Binding Proteins Haplotypes Intranuclear Inclusion Bodies Sequence Analysis, DNA Chromosome Fragility Phenotype Muscular Dystrophy, Oculopharyngeal Genetic Diseases, Inborn Nuclear Proteins Genetic Variation Models, Genetic Amyotrophic Lateral Sclerosis DNA Primers Genetic Markers Neurodegenerative Diseases Case-Control Studies Proteins DNA Repair Heterozygote DNA Mutational Analysis Genome, Human Peptides Transcription, Genetic Mice, Transgenic Receptors, Androgen RNA, Messenger DNA-Binding Proteins Promoter Regions, Genetic Amino Acid Sequence Chromosome Mapping Genes, Dominant Dinucleotide Repeats Genetic Linkage DNA Replication Myoclonic Epilepsies, Progressive MutS Homolog 2 Protein Saccharomyces cerevisiae Genetic Testing Repetitive Sequences, Amino Acid Cell Line Nucleic Acid Heteroduplexes Disease Models, Animal Sequence Deletion Recombination, Genetic Chromosomes, Human, X

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