Metaphase nucleic comparative genomic hybridization. Medical search. Frequent questions

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Anatomy37

Chromosomes, Artificial, Bacterial Chromosomes, Human Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 12 Chromosomes Chromosomes, Human, Pair 16 Polar Bodies Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 18 Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 14 Chromosomes, Human, X Ring Chromosomes Cell Line, Tumor Chromosomes, Artificial, P1 Bacteriophage Chromosomes, Human, Pair 19 Isochromosomes Chromosomes, Human, Pair 10 Tumor Cells, Cultured Oocytes Spindle Apparatus Blastomeres X Chromosome Chromosomes, Human, Y Cell Line

Organisms2

Brucella ovis Clostridium botulinum type B

Diseases72

Chromosome Aberrations Chromosome Deletion Aneuploidy Chromosome Disorders Intellectual Disability Genomic Instability Chromosome Duplication Abnormalities, Multiple Chromosome Breakage Translocation, Genetic Chromosomal Instability Breast Neoplasms Ring Chromosomes Keratoacanthoma Abnormal Karyotype Trisomy Carcinoma, Squamous Cell Leiomyosarcoma Lymphoma, Large B-Cell, Diffuse Facies Histiocytoma, Benign Fibrous Syndrome Isochromosomes Carcinoma in Situ Ependymoma Uveal Neoplasms Adenocarcinoma Skin Neoplasms Astrocytoma Monosomy Carcinoma, Ductal, Breast Disease Progression Mental Retardation, X-Linked Medulloblastoma Brain Neoplasms Dermatofibrosarcoma Neoplasms Neoplasms, Plasma Cell Liver Neoplasms Oligodendroglioma Hernia, Diaphragmatic Craniofacial Abnormalities Melanoma Lymphoma, B-Cell Adenoma Lung Neoplasms Carcinoma Supratentorial Neoplasms Apraxias Urinary Bladder Neoplasms Paraganglioma Ovarian Neoplasms Genetic Diseases, Inborn Sex Chromosome Aberrations Cerebellar Neoplasms Mesothelioma Meningioma Nerve Sheath Neoplasms Neuroblastoma Kidney Neoplasms Carcinoma, Hepatocellular Meningeal Neoplasms Stomach Neoplasms Neoplasm Metastasis Microcephaly Glioblastoma Chondrosarcoma Soft Tissue Neoplasms Neuroectodermal Tumors, Primitive Precancerous Conditions Trophoblastic Tumor, Placental Site Genetic Predisposition to Disease

Chemicals and Drugs19

DNA, Neoplasm DNA DNA, Bacterial DNA Probes RNA, Messenger Formaldehyde Genetic Markers Fixatives Oligonucleotide Probes Neoplasm Proteins DNA Primers DNA, Complementary Tumor Markers, Biological DNA-Binding Proteins Oncogene Proteins Nuclear Proteins Transcription Factors Cell Cycle Proteins Tumor Suppressor Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment46

Comparative Genomic Hybridization Nucleic Acid Hybridization In Situ Hybridization, Fluorescence Oligonucleotide Array Sequence Analysis Karyotyping Chromosome Mapping Cytogenetic Analysis In Situ Hybridization Gene Expression Profiling Chromosome Banding Sequence Analysis, DNA Spectral Karyotyping Polymerase Chain Reaction Microarray Analysis Cluster Analysis Chromosome Painting Paraffin Embedding Nucleic Acid Amplification Techniques Preimplantation Diagnosis Prognosis Models, Genetic Hybridization, Genetic Blotting, Southern Microdissection Genetic Testing Reverse Transcriptase Polymerase Chain Reaction Immunohistochemistry Reproducibility of Results DNA Mutational Analysis Prenatal Diagnosis Sequence Alignment Facies Physical Chromosome Mapping Cloning, Molecular Sensitivity and Specificity Neoplasm Staging Pedigree Tissue Fixation Genetic Association Studies Tissue Array Analysis Frozen Sections Genetic Techniques Survival Analysis Markov Chains Bacterial Typing Techniques DNA Fingerprinting

Psychiatry and Psychology4

Intellectual Disability Developmental Disabilities Autistic Disorder Apraxias

Phenomena and Processes115

Nucleic Acid Hybridization Chromosome Aberrations Metaphase Gene Dosage DNA Copy Number Variations Chromosome Deletion Chromosomes, Artificial, Bacterial Gene Amplification Chromosomes, Human Genome, Human Aneuploidy Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 1 Genome, Bacterial Chromosomes, Human, Pair 3 Gene Deletion Genomic Instability Chromosome Duplication Chromosomes, Human, Pair 17 Loss of Heterozygosity Chromosomes, Human, Pair 11 Genome Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 13 Gene Duplication Chromosomes, Human, Pair 6 Base Sequence Phylogeny Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 12 Chromosomes Chromosomes, Human, Pair 16 Genetic Variation Chromosomes, Human, Pair 15 Allelic Imbalance Chromosome Breakpoints Chromosomes, Human, Pair 2 Phenotype Chromosomes, Human, Pair 22 Chromosome Breakage Karyotype Translocation, Genetic Chromosomal Instability Segmental Duplications, Genomic Gene Expression Regulation, Neoplastic Chromosomes, Human, Pair 18 Ploidies Mutation Genomic Islands Sequence Deletion Chromosomes, Human, Pair 5 Genes, Neoplasm Microsatellite Repeats Chromosomes, Human, Pair 14 Evolution, Molecular Species Specificity Chromosomes, Human, X Ring Chromosomes Multigene Family Abnormal Karyotype Chromosomes, Artificial, P1 Bacteriophage Algorithms Hybridization, Genetic Trisomy Genetic Markers Interphase Gene Rearrangement Chromosomes, Human, Pair 19 Amino Acid Sequence Genotype Genes, Tumor Suppressor Isochromosomes Oncogenes Chromosomes, Human, Pair 10 Genes, Bacterial Mitosis Gene Fusion Genomic Structural Variation Meiosis Polymorphism, Single Nucleotide Sensitivity and Specificity Monosomy Gene Order Gene Expression Anaphase Exons Pregnancy Homozygote Diploidy Genetic Heterogeneity Synteny Genomic Library Transcription, Genetic Mosaicism Genes, myc DNA Methylation Genes, p53 X Chromosome Sequence Homology, Nucleic Acid Genetic Loci Genes, Duplicate Sex Chromosome Aberrations Alleles Genes, p16 Genes, erbB-2 Chromosomes, Human, Y Open Reading Frames Markov Chains Exome Genetic Linkage Polymorphism, Genetic Virulence Genetic Predisposition to Disease

Disciplines and Occupations4

Genomics Cytogenetics Immunohistochemistry Computational Biology

Anthropology, Education, Sociology and Social Phenomena1

DNA Fingerprinting

Information Science9

Molecular Sequence Data Base Sequence Phylogeny Algorithms Amino Acid Sequence Software Databases, Genetic Image Processing, Computer-Assisted User-Computer Interface

Named Groups1

Infant, Newborn

Health Care6

Cluster Analysis Genetic Testing Reproducibility of Results Sensitivity and Specificity Survival Analysis Markov Chains

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

Comparative Genomic Hybridization Nucleic Acid Hybridization Chromosome Aberrations Metaphase Gene Dosage In Situ Hybridization, Fluorescence Oligonucleotide Array Sequence Analysis DNA Copy Number Variations Karyotyping Chromosome Deletion Chromosomes, Artificial, Bacterial Gene Amplification Chromosomes, Human DNA, Neoplasm Genome, Human Chromosome Mapping Genomics Aneuploidy Cytogenetic Analysis Cytogenetics Chromosomes, Human, Pair 20 In Situ Hybridization Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 1 Gene Expression Profiling Chromosome Disorders Chromosome Banding Genome, Bacterial Sequence Analysis, DNA Chromosomes, Human, Pair 3 Gene Deletion Intellectual Disability Genomic Instability Chromosome Duplication Chromosomes, Human, Pair 17 Loss of Heterozygosity Spectral Karyotyping Chromosomes, Human, Pair 11 Genome Molecular Sequence Data Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 13 Gene Duplication Chromosomes, Human, Pair 6 Base Sequence Polymerase Chain Reaction Phylogeny Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 12 Chromosomes Microarray Analysis Chromosomes, Human, Pair 16 Polar Bodies Genetic Variation Chromosomes, Human, Pair 15 Allelic Imbalance Chromosome Breakpoints Cluster Analysis Abnormalities, Multiple Chromosome Painting Chromosomes, Human, Pair 2 Paraffin Embedding Phenotype Chromosomes, Human, Pair 22 Chromosome Breakage Karyotype Translocation, Genetic Chromosomal Instability Segmental Duplications, Genomic Gene Expression Regulation, Neoplastic DNA Chromosomes, Human, Pair 18 Ploidies Mutation Genomic Islands Sequence Deletion Chromosomes, Human, Pair 5 Nucleic Acid Amplification Techniques Genes, Neoplasm Microsatellite Repeats Preimplantation Diagnosis Chromosomes, Human, Pair 14 Evolution, Molecular Species Specificity DNA, Bacterial Chromosomes, Human, X DNA Probes Breast Neoplasms Ring Chromosomes Keratoacanthoma Cell Line, Tumor Multigene Family Prognosis Abnormal Karyotype Chromosomes, Artificial, P1 Bacteriophage Algorithms Models, Genetic Hybridization, Genetic RNA, Messenger

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