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

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Anatomy16

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

Organisms1

Pan troglodytes

Diseases16

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

Chemicals and Drugs7

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment26

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

Psychiatry and Psychology3

46, XX Disorders of Sex Development Autistic Disorder Intellectual Disability

Phenomena and Processes66

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

Disciplines and Occupations4

Genomics Genetics, Population Computational Biology HapMap Project

Information Science6

Base Sequence Molecular Sequence Data Algorithms Phylogeny Software Databases, Genetic

Named Groups2

Asian Continental Ancestry Group European Continental Ancestry Group

Health Care6

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

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 Gene Duplication Oligonucleotide Array Sequence Analysis Comparative Genomic Hybridization Genome, Human Genetic Variation Base Sequence Polymerase Chain Reaction Segmental Duplications, Genomic Molecular Sequence Data Polymorphism, Single Nucleotide Chromosome Aberrations Genomics Chromosome Duplication Sequence Analysis, DNA Genome Nucleic Acid Hybridization Chromosomes, Artificial, Bacterial Chromosome Mapping In Situ Hybridization, Fluorescence Genome-Wide Association Study Gene Amplification Chromosomes, Human Genotype DNA, Neoplasm Algorithms Gene Expression Profiling Genetic Predisposition to Disease Evolution, Molecular Gene Deletion Genomic Structural Variation Phenotype Genetic Loci Models, Genetic Hereditary Breast and Ovarian Cancer Syndrome DNA, Mitochondrial Alleles Chromosome Deletion Phylogeny Genotyping Techniques DNA Mutation Software Chromosomes, Human, Pair 1 Databases, Genetic Multigene Family Karyotyping Reproducibility of Results Chromosomes, Human, Pair 8 Chromosomes, Mammalian 46, XX Disorders of Sex Development Markov Chains Chromosomes, Human, X Chromosomes, Human, Pair 16 Cluster Analysis Autistic Disorder Chromosomes, Human, Pair 22 Exome Loss of Heterozygosity Genes, Neoplasm Sequence Deletion Haplotypes INDEL Mutation Genetics, Population Computational Biology Pseudogenes Nucleic Acid Amplification Techniques HapMap Project High-Throughput Nucleotide Sequencing Case-Control Studies Genomic Instability Aneuploidy Chromosomes, Human, Pair 17 Asian Continental Ancestry Group Chromosomes, Human, Pair 2 Gene Expression Regulation, Neoplastic Genetic Association Studies Real-Time Polymerase Chain Reaction Pedigree Gene Frequency Chromosomes, Human, Pair 6 Species Specificity Microarray Analysis Smith-Magenis Syndrome Chromosomes, Human, Pair 20 Inheritance Patterns DNA Mutational Analysis Exons Tandem Repeat Sequences DNA, Viral Chromosomes Hypertrichosis Cell Line, Tumor Polymorphism, Genetic Chromosome Breakage Chromosomes, Human, Pair 7 Complement C4a Pan troglodytes

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