Study 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, Pair 16 Chromosomes, Human, Pair 22 Chromosomes, Human, X Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 17 Cell Line, Tumor Chromosomes Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 3

Organisms1

Pan troglodytes

Diseases13

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

Chemicals and Drugs7

DNA, Neoplasm DNA, Mitochondrial DNA RNA, Messenger DNA, Viral Complement C4a beta-Defensins

Analytical, Diagnostic and Therapeutic Techniques and Equipment26

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

Psychiatry and Psychology2

46, XX Disorders of Sex Development Autistic Disorder

Phenomena and Processes60

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

Disciplines and Occupations4

Genomics Computational Biology Genetics, Population HapMap Project

Information Science6

Base Sequence Molecular Sequence Data Algorithms Databases, Genetic Software Phylogeny

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

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