Dna sequence variants. Medical search. Frequent questions

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Anatomy15

Cell Line Chromosomes, Human, Pair 9 Chromosomes, Human, X Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 8 Cells, Cultured Nucleosomes Chromosomes Centromere Cell Line, Tumor Chromatin Cell Nucleus CHO Cells

Organisms7

Viroids Escherichia coli Muridae Cricetinae Saccharomyces cerevisiae HIV-1 Bacteriophage lambda

Diseases22

Genetic Predisposition to Disease Anophthalmos Microphthalmos Glaucoma, Open-Angle Exfoliation Syndrome Vitelliform Macular Dystrophy Dystonic Disorders Puberty, Delayed Prostatic Neoplasms Keratoconus Genetic Diseases, Inborn Hirschsprung Disease Breast Neoplasms Usher Syndromes Neoplastic Syndromes, Hereditary Heart Septal Defects Chromosome Deletion Hearing Loss Retinitis Pigmentosa Macular Degeneration Retinal Diseases Syndrome

Chemicals and Drugs59

DNA Toll-Like Receptor 10 DNA Primers DNA, Viral DNA Restriction Enzymes DNA, Mitochondrial DNA, Bacterial Toll-Like Receptor 6 Eye Proteins DNA-Binding Proteins Transcription Factors RNA, Messenger Genetic Markers Untranslated Regions Codon Codon, Nonsense Bacterial Proteins BRCA2 Protein BRCA1 Protein Membrane Proteins DNA, Neoplasm DNA, Recombinant Oligonucleotide Probes DNA, Fungal DNA, Complementary Protein Isoforms 5' Untranslated Regions Transcription Factor TFIIIA DNA Transposable Elements Proteins Toll-Like Receptor 1 Recombinant Proteins 3' Untranslated Regions Carrier Proteins Nuclear Proteins RNA DNA, Satellite DNA, Ribosomal DNA Probes Homeodomain Proteins Oligodeoxyribonucleotides RNA, Viral Nerve Tissue Proteins Proto-Oncogene Proteins c-ret DNA, Plant Oligonucleotides Deoxyribonucleases, Type II Site-Specific ATP-Binding Cassette Transporters Nucleosomes DNA, Ribosomal Spacer Glycoproteins Viral Proteins Histones Recombinant Fusion Proteins Chromatin DNA, Chloroplast Repressor Proteins Deoxyribonuclease I Neoplasm Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment39

Sequence Analysis, DNA DNA Mutational Analysis Polymerase Chain Reaction Pedigree Cloning, Molecular Case-Control Studies Chromosome Mapping Sequence Alignment Genome-Wide Association Study Nucleic Acid Hybridization Genetic Testing Heteroduplex Analysis Models, Genetic Genetic Association Studies Amino Acid Substitution Restriction Mapping High-Throughput Nucleotide Sequencing Likelihood Functions Cohort Studies Sequence Analysis Models, Molecular Nucleic Acid Denaturation Risk Factors Transfection Blotting, Southern Mutagenesis, Site-Directed Reverse Transcriptase Polymerase Chain Reaction Molecular Sequence Annotation Oligonucleotide Array Sequence Analysis Electrophoresis, Polyacrylamide Gel Chromatography, High Pressure Liquid Electrophoresis, Capillary Individualized Medicine Sensitivity and Specificity Gene Expression Profiling Sequence Analysis, Protein Models, Statistical Odds Ratio Reproducibility of Results

Psychiatry and Psychology1

Phenomena and Processes114

Genetic Variation Polymorphism, Single Nucleotide Genotype Base Sequence Mutation Genetic Predisposition to Disease Amino Acid Sequence Alleles Exons Haplotypes Polymorphism, Genetic Gene Frequency Mutation, Missense Genomic Structural Variation Phenotype Phylogeny Exome Polymorphism, Single-Stranded Conformational Sequence Homology, Nucleic Acid Introns Nucleic Acid Hybridization Genome, Human Heterozygote Genes Promoter Regions, Genetic Nucleic Acid Conformation Species Specificity Repetitive Sequences, Nucleic Acid Point Mutation Transcription, Genetic Alternative Splicing Plasmids Genetic Linkage Linkage Disequilibrium Homozygote Germ-Line Mutation Evolution, Molecular Amino Acid Substitution Transition Temperature Sequence Homology, Amino Acid Genes, Bacterial Recombination, Genetic Binding Sites Genetic Markers Conserved Sequence Open Reading Frames Untranslated Regions Sequence Deletion Genetic Loci Polymorphism, Restriction Fragment Length Codon Frameshift Mutation Codon, Nonsense INDEL Mutation Gene Expression Regulation Genetic Heterogeneity Regulatory Sequences, Nucleic Acid Consensus Sequence Genome Genes, Recessive Algorithms Protein Binding Chromosomes, Human, Pair 9 Nucleic Acid Denaturation Multigene Family Quantitative Trait Loci RNA Splicing 5' Untranslated Regions DNA Transposable Elements Transfection Genes, BRCA1 Selection, Genetic Genome, Viral Chromosomes, Human, X Chromosomes, Human, Pair 15 Inheritance Patterns Protein Structure, Tertiary 3' Untranslated Regions Genes, Viral Gene Expression Base Composition Genes, BRCA2 Penetrance Kinetics Gene Deletion Biological Evolution Founder Effect Chromosomes, Human, Pair 1 DNA, Satellite Microsatellite Repeats Operon Structure-Activity Relationship Chromosome Deletion Genes, Regulator Consanguinity Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 8 Sensitivity and Specificity Genes, Dominant Nucleosomes Gene Amplification Mutagenesis DNA Replication Gene Library Molecular Weight Chromosomes Nucleic Acid Renaturation Centromere Genes, Fungal Odds Ratio Protein Conformation Chromatin Substrate Specificity Lod Score

Disciplines and Occupations4

Computational Biology Genomics Genetics, Population Individualized Medicine

Anthropology, Education, Sociology and Social Phenomena2

Demography Family

Information Science10

Base Sequence Molecular Sequence Data Amino Acid Sequence Phylogeny Software Algorithms Databases, Genetic Molecular Sequence Annotation Internet Computer Simulation

Named Groups4

European Continental Ancestry Group Asian Continental Ancestry Group African Continental Ancestry Group African Americans

Health Care14

Case-Control Studies Genome-Wide Association Study Genetic Testing Age of Onset Likelihood Functions Knowledge Management Cohort Studies Risk Factors Family Health Demography Sensitivity and Specificity Models, Statistical Odds Ratio Reproducibility of Results

Geographicals6

Iceland Europe Jordan Pakistan China Germany

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care Geographicals

Genetic Variation Sequence Analysis, DNA Polymorphism, Single Nucleotide Genotype Base Sequence Molecular Sequence Data Mutation DNA Mutational Analysis Genetic Predisposition to Disease Amino Acid Sequence DNA Alleles Polymerase Chain Reaction Exons Haplotypes Polymorphism, Genetic Gene Frequency Mutation, Missense Pedigree Anophthalmos Genomic Structural Variation Phenotype Cloning, Molecular Phylogeny Exome Polymorphism, Single-Stranded Conformational Case-Control Studies Chromosome Mapping Toll-Like Receptor 10 Sequence Homology, Nucleic Acid Introns DNA Primers Sequence Alignment Genome-Wide Association Study Nucleic Acid Hybridization Genome, Human Genetic Testing Heterozygote Microphthalmos Genes Viroids Promoter Regions, Genetic DNA, Viral Nucleic Acid Conformation DNA Restriction Enzymes Heteroduplex Analysis Species Specificity Repetitive Sequences, Nucleic Acid Point Mutation Transcription, Genetic DNA, Mitochondrial DNA, Bacterial Alternative Splicing Plasmids Genetic Linkage Linkage Disequilibrium Models, Genetic Genetic Association Studies Homozygote Toll-Like Receptor 6 Germ-Line Mutation Evolution, Molecular Amino Acid Substitution Eye Proteins Transition Temperature DNA-Binding Proteins Glaucoma, Open-Angle Escherichia coli Software Sequence Homology, Amino Acid Genes, Bacterial Recombination, Genetic Binding Sites Transcription Factors RNA, Messenger Genetic Markers Cell Line Conserved Sequence Restriction Mapping Exfoliation Syndrome Open Reading Frames Untranslated Regions Vitelliform Macular Dystrophy Iceland Sequence Deletion Genetic Loci Polymorphism, Restriction Fragment Length Codon High-Throughput Nucleotide Sequencing Computational Biology Frameshift Mutation Codon, Nonsense INDEL Mutation European Continental Ancestry Group Gene Expression Regulation Bacterial Proteins BRCA2 Protein Age of Onset BRCA1 Protein Likelihood Functions

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