Fluorescence in situ hybr comparative genomic hybridization. Medical search. Frequent questions

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Anatomy34

Chromosomes, Artificial, Bacterial Chromosomes, Human Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 8 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, Human, Pair 16 Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 2 Polar Bodies Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 18 Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 14 Chromosomes, Human, X Cell Line, Tumor Ring Chromosomes Chromosomes Chromosomes, Artificial, P1 Bacteriophage Chromosomes, Human, Pair 19 Tumor Cells, Cultured Chromosomes, Human, Pair 10 Isochromosomes Cell Line Chromosomes, Human, Y X Chromosome

Organisms2

Brucella ovis Clostridium botulinum type B

Diseases71

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

Chemicals and Drugs20

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment50

Comparative Genomic Hybridization Nucleic Acid Hybridization In Situ Hybridization, Fluorescence Oligonucleotide Array Sequence Analysis Karyotyping In Situ Hybridization Chromosome Mapping Cytogenetic Analysis Spectrometry, Fluorescence Gene Expression Profiling Sequence Analysis, DNA Chromosome Banding Spectral Karyotyping Polymerase Chain Reaction Microarray Analysis Cluster Analysis Paraffin Embedding Microscopy, Fluorescence Chromosome Painting Nucleic Acid Amplification Techniques Preimplantation Diagnosis Fluorescence Polarization Prognosis Models, Genetic Immunohistochemistry Microdissection Reproducibility of Results Blotting, Southern Hybridization, Genetic Reverse Transcriptase Polymerase Chain Reaction Genetic Testing DNA Mutational Analysis Sequence Alignment Sensitivity and Specificity Prenatal Diagnosis Facies Physical Chromosome Mapping Cloning, Molecular Fluorescence Resonance Energy Transfer Neoplasm Staging Pedigree Tissue Fixation Tissue Array Analysis Genetic Association Studies 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 Processes114

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

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 Image Processing, Computer-Assisted Databases, Genetic User-Computer Interface

Named Groups1

Infant, Newborn

Health Care6

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

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