Diagnostic nucleic comparative genomic hybridization. Medical search. Frequent questions

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Anatomy33

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 4 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 15 Polar Bodies Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 18 Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 14 Chromosomes, Human, X Cell Line, Tumor Chromosomes, Artificial, P1 Bacteriophage Ring Chromosomes Chromosomes Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 10 Tumor Cells, Cultured Isochromosomes Chromosomes, Human, Y X Chromosome

Organisms2

Brucella ovis Clostridium botulinum type B

Diseases75

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

Chemicals and Drugs18

DNA, Neoplasm DNA DNA, Bacterial DNA Probes Formaldehyde RNA, Messenger Fixatives Genetic Markers Oligonucleotide Probes Tumor Markers, Biological Neoplasm Proteins DNA Primers DNA, Complementary Oncogene Proteins Transcription Factors DNA-Binding Proteins Tumor Suppressor Proteins RNA, Ribosomal, 16S

Analytical, Diagnostic and Therapeutic Techniques and Equipment50

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 Sequence Analysis, DNA Chromosome Banding Spectral Karyotyping Polymerase Chain Reaction Microarray Analysis Cluster Analysis Paraffin Embedding Chromosome Painting Nucleic Acid Amplification Techniques Preimplantation Diagnosis Sensitivity and Specificity Prognosis Reproducibility of Results Models, Genetic Microdissection Genetic Testing Hybridization, Genetic Blotting, Southern Reverse Transcriptase Polymerase Chain Reaction Immunohistochemistry DNA Mutational Analysis Prenatal Diagnosis Facies Sequence Alignment Physical Chromosome Mapping Neoplasm Staging Cloning, Molecular Pedigree Tissue Array Analysis Genetic Association Studies Tissue Fixation Frozen Sections Molecular Diagnostic Techniques Genetic Techniques Survival Analysis Biopsy Markov Chains Bacterial Typing Techniques Predictive Value of Tests DNA Fingerprinting Diagnostic Errors

Psychiatry and Psychology4

Intellectual Disability Developmental Disabilities Autistic Disorder Apraxias

Phenomena and Processes112

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

Disciplines and Occupations4

Genomics Cytogenetics Immunohistochemistry Computational Biology

Anthropology, Education, Sociology and Social Phenomena1

DNA Fingerprinting

Information Science10

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

Named Groups1

Infant, Newborn

Health Care8

Cluster Analysis Sensitivity and Specificity Reproducibility of Results Genetic Testing Survival Analysis Markov Chains Predictive Value of Tests Diagnostic Errors

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

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