Expansions trinucleotide. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy10

Intranuclear Inclusion Bodies Chromosomes, Human, X Cells, Cultured X Chromosome Cell Line Brain CD8-Positive T-Lymphocytes Clone Cells CD4-Positive T-Lymphocytes Hematopoietic Stem Cells

Organisms4

Mice, Transgenic Saccharomyces cerevisiae Escherichia coli Mice, Inbred C57BL

Diseases19

Friedreich Ataxia Fragile X Syndrome Huntington Disease Spinocerebellar Degenerations Machado-Joseph Disease Heredodegenerative Disorders, Nervous System Genomic Instability Muscular Dystrophy, Oculopharyngeal Chromosome Fragility Anticipation, Genetic Cerebellar Ataxia Genetic Diseases, Inborn Neurodegenerative Diseases Disease Models, Animal Muscular Atrophy, Spinal Ataxia Nervous System Diseases Intellectual Disability Myotonic Dystrophy

Chemicals and Drugs36

Fragile X Mental Retardation Protein DNA Nerve Tissue Proteins Oligonucleotides Iron-Binding Proteins Flap Endonucleases RNA-Binding Proteins Peptides Receptors, Androgen Oligodeoxyribonucleotides Nucleic Acid Heteroduplexes Nucleotides Nuclear Proteins DNA Primers RNA, Messenger RNA Guanine Oligoribonucleotides Genetic Markers Codon Polydeoxyribonucleotides DNA-Binding Proteins DNA, Satellite MutS Homolog 2 Protein Transcription Factors Saccharomyces cerevisiae Proteins DNA, Plant Proteins Endodeoxyribonucleases Cytosine DNA, Complementary DNA, Fungal DNA, Single-Stranded RNA, Transfer Protein-Serine-Threonine Kinases Adenine

Analytical, Diagnostic and Therapeutic Techniques and Equipment21

Polymerase Chain Reaction Palatal Expansion Technique Pedigree Sequence Analysis, DNA Models, Genetic Gene Knock-In Techniques Tissue Expansion Chromosome Mapping Disease Models, Animal Models, Molecular DNA Mutational Analysis Nucleic Acid Denaturation Blotting, Southern Cloning, Molecular Genetic Testing Models, Biological Lymphocyte Activation Circular Dichroism Magnetic Resonance Spectroscopy Sequence Alignment Cell Culture Techniques

Psychiatry and Psychology3

Huntington Disease Fathers Intellectual Disability

Phenomena and Processes72

Trinucleotide Repeats Trinucleotide Repeat Expansion Base Sequence Repetitive Sequences, Nucleic Acid Nucleic Acid Conformation Alleles Microsatellite Repeats Genomic Instability DNA Repeat Expansion Mutation Chromosome Fragility Polymorphism, Genetic Anticipation, Genetic Minisatellite Repeats Inverted Repeat Sequences Phenotype Genetic Variation Chromosome Fragile Sites Dinucleotide Repeats Tandem Repeat Sequences DNA Repair Transcription, Genetic Mosaicism Genotype Amino Acid Sequence DNA Replication Chromosomes, Human, X Genome, Human Evolution, Molecular Genetic Markers Codon Heterozygote Sequence Tagged Sites Gene Frequency Exons Expressed Sequence Tags Phylogeny DNA, Satellite Sequence Deletion Genes, Dominant Point Mutation Mutagenesis Templates, Genetic Base Pairing X Chromosome Nucleic Acid Denaturation Cell Proliferation Binding Sites Haplotypes Recombination, Genetic Genetic Loci Gene Expression Kinetics Genome, Fungal Promoter Regions, Genetic Cell Differentiation DNA, Single-Stranded Species Specificity Base Composition Genome, Plant Lymphocyte Activation Base Pair Mismatch Thermodynamics Genetic Linkage Consensus Sequence Sequence Homology, Nucleic Acid Conserved Sequence Gene Expression Regulation Open Reading Frames Substrate Specificity Sequence Homology, Amino Acid Introns

Disciplines and Occupations1

Genetics, Population

Anthropology, Education, Sociology and Social Phenomena1

Information Science4

Base Sequence Molecular Sequence Data Amino Acid Sequence Phylogeny

Named Groups1

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 Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care

Trinucleotide Repeats Trinucleotide Repeat Expansion Friedreich Ataxia Fragile X Syndrome Huntington Disease Spinocerebellar Degenerations Fragile X Mental Retardation Protein Base Sequence Repetitive Sequences, Nucleic Acid Machado-Joseph Disease Molecular Sequence Data Nucleic Acid Conformation Alleles Microsatellite Repeats DNA Nerve Tissue Proteins Heredodegenerative Disorders, Nervous System Genomic Instability DNA Repeat Expansion Mutation Muscular Dystrophy, Oculopharyngeal Oligonucleotides Iron-Binding Proteins Polymerase Chain Reaction Flap Endonucleases Chromosome Fragility Polymorphism, Genetic Palatal Expansion Technique Anticipation, Genetic RNA-Binding Proteins Cerebellar Ataxia Pedigree Minisatellite Repeats Genetic Diseases, Inborn Age of Onset Peptides Sequence Analysis, DNA Intranuclear Inclusion Bodies Inverted Repeat Sequences Models, Genetic Receptors, Androgen Oligodeoxyribonucleotides Phenotype Mice, Transgenic Genetic Variation Chromosome Fragile Sites Nucleic Acid Heteroduplexes Dinucleotide Repeats Neurodegenerative Diseases Nucleotides Nuclear Proteins DNA Primers Tandem Repeat Sequences DNA Repair Gene Knock-In Techniques Transcription, Genetic RNA, Messenger RNA Mosaicism Genotype Guanine Amino Acid Sequence DNA Replication Saccharomyces cerevisiae Chromosomes, Human, X Oligoribonucleotides Genome, Human Evolution, Molecular Tissue Expansion Chromosome Mapping Genetic Markers Codon Heterozygote Sequence Tagged Sites Polydeoxyribonucleotides DNA-Binding Proteins Gene Frequency Disease Models, Animal Exons Muscular Atrophy, Spinal Expressed Sequence Tags Ataxia Phylogeny Models, Molecular DNA, Satellite Sequence Deletion Cells, Cultured Genes, Dominant Point Mutation MutS Homolog 2 Protein Mutagenesis Transcription Factors Templates, Genetic Saccharomyces cerevisiae Proteins Base Pairing X Chromosome DNA Mutational Analysis Nucleic Acid Denaturation Genetics, Population Escherichia coli

No FAQ available that match "expansions trinucleotide"