Functional 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 Drugs10

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment27

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

Psychiatry and Psychology2

46, XX Disorders of Sex Development Autistic Disorder

Phenomena and Processes63

DNA Copy Number Variations Gene Dosage Genome, Human Genetic Variation Base Sequence Polymorphism, Single Nucleotide Gene Duplication Chromosome Aberrations Nucleic Acid Hybridization Segmental Duplications, Genomic Genome Chromosomes, Artificial, Bacterial Pseudogenes Genotype Gene Amplification Chromosomes, Human Algorithms Genetic Predisposition to Disease Genomic Structural Variation Genetic Loci Gene Deletion Phenotype Alleles Chromosome Duplication Evolution, Molecular Mutation Chromosome Deletion Chromosomes, Human, Pair 1 Phylogeny Chromosomes, Human, Pair 8 Markov Chains Chromosomes, Mammalian Genes, Neoplasm Exome Loss of Heterozygosity Haplotypes Sequence Deletion Chromosomes, Human, Pair 16 INDEL Mutation Chromosomes, Human, Pair 22 Chromosomes, Human, X Gene Expression Regulation, Neoplastic Gene Frequency Genomic Instability Species Specificity Multigene Family Aneuploidy Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 6 Polymorphism, Genetic Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 17 Inheritance Patterns Exons Recombination, Genetic Chromosomes Transcription, Genetic Gene Regulatory Networks Microsatellite Repeats Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 3 Gene Expression 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 Care7

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

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