Promoter fmr1 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 Fragile X Syndrome Spinocerebellar Degenerations Myotonic Dystrophy 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 Amyotrophic Lateral Sclerosis Neurodegenerative Diseases Ataxia Myoclonic Epilepsies, Progressive Disease Models, Animal

Chemicals and Drugs20

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment7

Pedigree Polymerase Chain Reaction Sequence Analysis, DNA Models, Genetic Disease Models, Animal DNA Mutational Analysis Chromosome Mapping

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes37

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

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Health Care1

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

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