Closely related 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 Cell Line, Tumor Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 17 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 Breast Neoplasms Chromosomal Instability

Chemicals and Drugs8

DNA, Neoplasm DNA, Mitochondrial DNA RNA, Messenger 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 Nucleic Acid Hybridization Sequence Analysis, DNA Genome-Wide Association Study Gene Expression Profiling Chromosome Mapping In Situ Hybridization, Fluorescence Models, Genetic Genotyping Techniques Reproducibility of Results Cluster Analysis Markov Chains Case-Control Studies Real-Time Polymerase Chain Reaction Karyotyping High-Throughput Nucleotide Sequencing Genetic Association Studies Nucleic Acid Amplification Techniques Microarray Analysis Pedigree Reverse Transcriptase Polymerase Chain Reaction 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 Nucleic Acid Hybridization Segmental Duplications, Genomic Genome Chromosomes, Artificial, Bacterial Gene Amplification Genotype Chromosomes, Human Algorithms Genetic Predisposition to Disease Genomic Structural Variation Gene Deletion Phenotype Genetic Loci Chromosome Duplication Alleles Chromosome Deletion Mutation Chromosomes, Human, Pair 1 Genes, Neoplasm Chromosomes, Human, Pair 8 Markov Chains Chromosomes, Mammalian Exome Loss of Heterozygosity Gene Expression Regulation, Neoplastic Haplotypes Evolution, Molecular Chromosomes, Human, Pair 16 INDEL Mutation Chromosomes, Human, Pair 22 Chromosomes, Human, X Sequence Deletion Genomic Instability Gene Frequency Aneuploidy Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 6 Phylogeny Multigene Family Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 17 Pseudogenes Species Specificity Inheritance Patterns Polymorphism, Genetic Gene Expression Chromosomes Exons Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 3 Transcription, Genetic 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 Cluster Analysis Markov Chains 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 Molecular Sequence Data Gene Duplication Chromosome Aberrations Genomics Nucleic Acid Hybridization Sequence Analysis, DNA Segmental Duplications, Genomic Genome-Wide Association Study Genome Chromosomes, Artificial, Bacterial Gene Expression Profiling Chromosome Mapping Gene Amplification Genotype DNA, Neoplasm Chromosomes, Human In Situ Hybridization, Fluorescence Algorithms Genetic Predisposition to Disease Genomic Structural Variation Gene Deletion Phenotype Genetic Loci Hereditary Breast and Ovarian Cancer Syndrome DNA, Mitochondrial Chromosome Duplication Alleles Models, Genetic Databases, Genetic Genotyping Techniques DNA Software Reproducibility of Results Cluster Analysis Chromosome Deletion Mutation Chromosomes, Human, Pair 1 Genes, Neoplasm 46, XX Disorders of Sex Development Chromosomes, Human, Pair 8 Markov Chains Chromosomes, Mammalian Exome Loss of Heterozygosity Gene Expression Regulation, Neoplastic Case-Control Studies Haplotypes Evolution, Molecular Computational Biology Real-Time Polymerase Chain Reaction Autistic Disorder Genetics, Population Karyotyping HapMap Project Chromosomes, Human, Pair 16 INDEL Mutation Chromosomes, Human, Pair 22 Chromosomes, Human, X Sequence Deletion High-Throughput Nucleotide Sequencing Genetic Association Studies Nucleic Acid Amplification Techniques Asian Continental Ancestry Group Microarray Analysis Genomic Instability Gene Frequency Aneuploidy Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 6 Phylogeny Multigene Family Cell Line, Tumor Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 17 Pseudogenes Pedigree Species Specificity Inheritance Patterns Reverse Transcriptase Polymerase Chain Reaction Hypertrichosis RNA, Messenger Smith-Magenis Syndrome DNA, Viral DNA Mutational Analysis Polymorphism, Genetic Complement C4a beta-Defensins Neoplasms Gene Expression Blotting, Southwestern

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