Mglur fmr1 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 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 Disease Models, Animal Myoclonic Epilepsies, Progressive

Chemicals and Drugs17

Fragile X Mental Retardation Protein Iron-Binding Proteins Nerve Tissue Proteins Flap Endonucleases DNA RNA-Binding Proteins Receptor, Metabotropic Glutamate 5 Nuclear Proteins Peptides Proteins Receptors, Androgen DNA Primers RNA, Messenger Genetic Markers MutS Homolog 2 Protein Nucleic Acid Heteroduplexes DNA-Binding Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment5

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

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes30

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

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 Spinocerebellar Ataxias Machado-Joseph Disease Base Sequence Heredodegenerative Disorders, Nervous System Nerve Tissue Proteins Genomic Instability Molecular Sequence Data Frontotemporal Dementia Flap Endonucleases Anticipation, Genetic Microsatellite Repeats DNA Nucleic Acid Conformation Inverted Repeat Sequences Minisatellite Repeats Pedigree Tandem Repeat Sequences RNA-Binding Proteins Cerebellar Ataxia Intranuclear Inclusion Bodies Age of Onset Chromosome Fragility Muscular Dystrophy, Oculopharyngeal Polymerase Chain Reaction Genetic Diseases, Inborn Receptor, Metabotropic Glutamate 5 Amyotrophic Lateral Sclerosis Polymorphism, Genetic Nuclear Proteins Neurodegenerative Diseases Phenotype Peptides Proteins DNA Repair Sequence Analysis, DNA Mice, Transgenic Receptors, Androgen Models, Genetic Ataxia Genotype DNA Primers Heterozygote Disease Models, Animal DNA Replication Genes, Dominant Transcription, Genetic Myoclonic Epilepsies, Progressive RNA, Messenger Genome, Human Exons Genetic Markers MutS Homolog 2 Protein Repetitive Sequences, Amino Acid Nucleic Acid Heteroduplexes Saccharomyces cerevisiae Amino Acid Sequence DNA-Binding Proteins Chromosomes, Human, X Gene Frequency

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