Alleles genes dna copy number variations. Medical search. Frequent questions

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Anatomy16

Chromosomes, Artificial, Bacterial Chromosomes, Human Chromosomes, Human, Pair 1 Chromosomes, Mammalian Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 16 Chromosomes, Human, X Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 20 Cell Line, Tumor Chromosomes Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 3

Organisms1

Pan troglodytes

Diseases14

Adenomatoid Tumor Chromosome Aberrations Genetic Predisposition to Disease Hereditary Breast and Ovarian Cancer Syndrome Chromosome Duplication Chromosome Deletion 46, XX Disorders of Sex Development Genomic Instability Aneuploidy Hypertrichosis Smith-Magenis Syndrome Neoplasms Chromosomal Instability Tetraploidy

Chemicals and Drugs7

DNA, Neoplasm DNA, Mitochondrial DNA DNA, Viral Complement C4a beta-Defensins DNA Primers

Analytical, Diagnostic and Therapeutic Techniques and Equipment27

Oligonucleotide Array Sequence Analysis Comparative Genomic Hybridization Polymerase Chain Reaction Sequence Analysis, DNA Nucleic Acid Hybridization Genome-Wide Association Study Chromosome Mapping In Situ Hybridization, Fluorescence Gene Expression Profiling Models, Genetic Genotyping Techniques Reproducibility of Results Case-Control Studies Markov Chains Cluster Analysis Karyotyping Genetic Association Studies High-Throughput Nucleotide Sequencing Nucleic Acid Amplification Techniques Real-Time Polymerase Chain Reaction Pedigree Microarray Analysis DNA Mutational Analysis Genetic Testing Blotting, Southwestern Reverse Transcriptase Polymerase Chain Reaction Cohort Studies

Psychiatry and Psychology2

46, XX Disorders of Sex Development Autistic Disorder

Phenomena and Processes60

DNA Copy Number Variations Gene Dosage Alleles Genome, Human Genetic Variation Base Sequence Polymorphism, Single Nucleotide Gene Duplication Chromosome Aberrations Genotype Segmental Duplications, Genomic Nucleic Acid Hybridization Genome Chromosomes, Artificial, Bacterial Gene Amplification Chromosomes, Human Genetic Predisposition to Disease Algorithms Phenotype Genomic Structural Variation Gene Deletion Genetic Loci Chromosome Duplication Mutation Gene Frequency Haplotypes Chromosome Deletion Chromosomes, Human, Pair 1 Chromosomes, Mammalian Chromosomes, Human, Pair 8 Loss of Heterozygosity Markov Chains Exome Genes, Neoplasm Polymorphism, Genetic INDEL Mutation Chromosomes, Human, Pair 16 Sequence Deletion Chromosomes, Human, X Chromosomes, Human, Pair 22 Gene Expression Regulation, Neoplastic Evolution, Molecular Genomic Instability Aneuploidy Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 20 Inheritance Patterns Species Specificity Pseudogenes Linkage Disequilibrium Microsatellite Repeats Phylogeny Chromosomes Exons Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 3 Chromosomal Instability Tetraploidy

Disciplines and Occupations4

Genomics Genetics, Population HapMap Project Computational Biology

Information Science6

Base Sequence Molecular Sequence Data Algorithms Software Databases, Genetic Phylogeny

Named Groups2

Asian Continental Ancestry Group European Continental Ancestry Group

Health Care7

Genome-Wide Association Study Reproducibility of Results Case-Control Studies Markov Chains Cluster Analysis Genetic Testing Cohort Studies

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Information Science Named Groups Health Care

DNA Copy Number Variations Gene Dosage Adenomatoid Tumor Oligonucleotide Array Sequence Analysis Comparative Genomic Hybridization Alleles Genome, Human Genetic Variation Polymerase Chain Reaction Base Sequence Polymorphism, Single Nucleotide Gene Duplication Molecular Sequence Data Chromosome Aberrations Genomics Genotype Sequence Analysis, DNA Segmental Duplications, Genomic Nucleic Acid Hybridization Genome-Wide Association Study Genome Chromosomes, Artificial, Bacterial Chromosome Mapping Gene Amplification DNA, Neoplasm Chromosomes, Human Genetic Predisposition to Disease In Situ Hybridization, Fluorescence Algorithms Gene Expression Profiling Phenotype Genomic Structural Variation Gene Deletion Genetic Loci Hereditary Breast and Ovarian Cancer Syndrome DNA, Mitochondrial Chromosome Duplication Models, Genetic Genotyping Techniques Mutation Gene Frequency DNA Haplotypes Chromosome Deletion Software Chromosomes, Human, Pair 1 Reproducibility of Results Databases, Genetic 46, XX Disorders of Sex Development Genetics, Population Chromosomes, Mammalian Case-Control Studies Chromosomes, Human, Pair 8 Loss of Heterozygosity Markov Chains Exome Genes, Neoplasm Cluster Analysis Polymorphism, Genetic Asian Continental Ancestry Group Autistic Disorder HapMap Project Karyotyping INDEL Mutation Genetic Association Studies Chromosomes, Human, Pair 16 Sequence Deletion Chromosomes, Human, X Chromosomes, Human, Pair 22 High-Throughput Nucleotide Sequencing Nucleic Acid Amplification Techniques Gene Expression Regulation, Neoplastic Evolution, Molecular Real-Time Polymerase Chain Reaction Genomic Instability Pedigree Computational Biology Aneuploidy Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 6 Microarray Analysis Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 20 Inheritance Patterns DNA Mutational Analysis Cell Line, Tumor Hypertrichosis Species Specificity Pseudogenes DNA, Viral Complement C4a Smith-Magenis Syndrome European Continental Ancestry Group Linkage Disequilibrium beta-Defensins Microsatellite Repeats Phylogeny Chromosomes Genetic Testing Blotting, Southwestern

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