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

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Anatomy2

Intranuclear Inclusion Bodies 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 Chromosome Fragility Muscular Dystrophy, Oculopharyngeal Genetic Diseases, Inborn Genetic Predisposition to Disease Amyotrophic Lateral Sclerosis Neurodegenerative Diseases Myoclonic Epilepsies, Progressive Disease Models, Animal

Chemicals and Drugs19

Fragile X Mental Retardation Protein Iron-Binding Proteins Receptors, KIR3DL2 HLA-DQ Antigens Nerve Tissue Proteins DNA Flap Endonucleases Receptors, IgG RNA-Binding Proteins Nuclear Proteins Genetic Markers Proteins DNA Primers Peptides Receptors, Androgen DNA-Binding Proteins RNA, Messenger MutS Homolog 2 Protein Nucleic Acid Heteroduplexes

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

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

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes38

Trinucleotide Repeat Expansion Trinucleotide Repeats DNA Repeat Expansion Alleles Polymorphism, Genetic Base Sequence Mutation Gene Frequency Repetitive Sequences, Nucleic Acid Polymorphism, Single Nucleotide Genotype Haplotypes Genetic Variation Amino Acid Sequence Microsatellite Repeats Genomic Instability Minisatellite Repeats Anticipation, Genetic Tandem Repeat Sequences Nucleic Acid Conformation Inverted Repeat Sequences Chromosome Fragility Major Histocompatibility Complex Genetic Predisposition to Disease Phenotype Genetic Markers DNA Repair Heterozygote Exons Genome, Human Genes, Dominant Transcription, Genetic DNA Replication Repetitive Sequences, Amino Acid Promoter Regions, Genetic Dinucleotide Repeats Genetic Linkage 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 Spinocerebellar Degenerations Alleles Myotonic Dystrophy Fragile X Syndrome Polymorphism, Genetic Huntington Disease Fragile X Mental Retardation Protein Iron-Binding Proteins Receptors, KIR3DL2 Base Sequence Molecular Sequence Data Mutation Gene Frequency Repetitive Sequences, Nucleic Acid Polymerase Chain Reaction Polymorphism, Single Nucleotide Spinocerebellar Ataxias Genotype Haplotypes Machado-Joseph Disease HLA-DQ Antigens Genetic Variation Heredodegenerative Disorders, Nervous System Sequence Analysis, DNA Amino Acid Sequence Nerve Tissue Proteins Microsatellite Repeats DNA Genomic Instability Frontotemporal Dementia Flap Endonucleases Minisatellite Repeats Anticipation, Genetic Pedigree Tandem Repeat Sequences Nucleic Acid Conformation Inverted Repeat Sequences Age of Onset Receptors, IgG Cerebellar Ataxia Intranuclear Inclusion Bodies Chromosome Fragility Major Histocompatibility Complex Muscular Dystrophy, Oculopharyngeal Genetic Diseases, Inborn Genetic Predisposition to Disease RNA-Binding Proteins Phenotype Amyotrophic Lateral Sclerosis Nuclear Proteins Neurodegenerative Diseases Models, Genetic Genetic Markers DNA Repair Proteins Case-Control Studies DNA Primers Peptides Heterozygote Exons Receptors, Androgen Genome, Human Mice, Transgenic Genes, Dominant DNA Mutational Analysis Transcription, Genetic DNA-Binding Proteins Chromosome Mapping DNA Replication Myoclonic Epilepsies, Progressive RNA, Messenger MutS Homolog 2 Protein Repetitive Sequences, Amino Acid Nucleic Acid Heteroduplexes Saccharomyces cerevisiae Promoter Regions, Genetic Dinucleotide Repeats Genetic Linkage Disease Models, Animal Genetic Testing Chromosomes, Human, X

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