Mutations gene comparative genomic hybridization. Medical search. Frequent questions

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Anatomy33

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, X Chromosomes, Human, Pair 14 Cell Line, Tumor Chromosomes Chromosomes, Artificial, P1 Bacteriophage Ring Chromosomes Chromosomes, Human, Pair 19 Tumor Cells, Cultured Chromosomes, Human, Pair 10 Isochromosomes Cell Line X Chromosome

Organisms3

Brucella ovis Escherichia coli Clostridium botulinum type B

Diseases69

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 Syndrome Carcinoma, Squamous Cell Facies Leiomyosarcoma Trisomy Adenocarcinoma Lymphoma, Large B-Cell, Diffuse Skin Neoplasms Histiocytoma, Benign Fibrous Uveal Neoplasms Carcinoma in Situ Ependymoma Astrocytoma Mental Retardation, X-Linked Disease Progression Neoplasms Isochromosomes Brain Neoplasms Carcinoma, Ductal, Breast Craniofacial Abnormalities Medulloblastoma Liver Neoplasms Genetic Predisposition to Disease Melanoma Lung Neoplasms Oligodendroglioma Monosomy Dermatofibrosarcoma Adenoma Genetic Diseases, Inborn Neoplasms, Plasma Cell Ovarian Neoplasms Hernia, Diaphragmatic Carcinoma Paraganglioma Lymphoma, B-Cell Apraxias Urinary Bladder Neoplasms Microcephaly Supratentorial Neoplasms Kidney Neoplasms Carcinoma, Hepatocellular Cerebellar Neoplasms Neuroblastoma Stomach Neoplasms Meningioma Mesothelioma Neoplasm Metastasis Colorectal Neoplasms Nerve Sheath Neoplasms Glioblastoma Meningeal Neoplasms Cell Transformation, Neoplastic Precancerous Conditions

Chemicals and Drugs19

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment45

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

Psychiatry and Psychology4

Intellectual Disability Developmental Disabilities Autistic Disorder Apraxias

Phenomena and Processes122

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 Mutation Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 8 Point Mutation Genome, Bacterial Gene Deletion Base Sequence Mutation, Missense Chromosomes, Human, Pair 3 Genomic Instability Loss of Heterozygosity Chromosomes, Human, Pair 17 Chromosome Duplication Genome Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 9 Gene Duplication Phylogeny Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 6 Genetic Variation Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 12 Phenotype Chromosomes, Human, Pair 16 Allelic Imbalance Chromosome Breakpoints Chromosomes, Human, Pair 15 Sequence Deletion Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 22 Microsatellite Repeats Gene Expression Regulation, Neoplastic Chromosome Breakage Germ-Line Mutation Segmental Duplications, Genomic Evolution, Molecular Chromosomal Instability Genes, Neoplasm Chromosomes, Human, Pair 18 Karyotype Genomic Islands Translocation, Genetic Ploidies Species Specificity Chromosomes, Human, Pair 5 Exons Genotype Chromosomes, Human, X Frameshift Mutation Chromosomes, Human, Pair 14 Amino Acid Sequence Multigene Family Abnormal Karyotype Chromosomes Algorithms Chromosomes, Artificial, P1 Bacteriophage Ring Chromosomes Genetic Markers Homozygote Hybridization, Genetic Alleles Genes, Bacterial Gene Rearrangement Heterozygote Genes, Tumor Suppressor Chromosomes, Human, Pair 19 Polymorphism, Single Nucleotide Trisomy Oncogenes Genes, p53 Gene Expression Chromosomes, Human, Pair 10 Transcription, Genetic Sensitivity and Specificity Genetic Heterogeneity Gene Fusion Genomic Structural Variation Gene Order Metaphase Isochromosomes Genetic Linkage Exome Genetic Predisposition to Disease Polymorphism, Genetic Monosomy Sequence Homology, Amino Acid Mosaicism Genes, BRCA1 Sequence Homology, Nucleic Acid DNA Methylation Mutation Rate Genomic Library Diploidy Synteny Genetic Loci Conserved Sequence Pregnancy Open Reading Frames X Chromosome Genes, myc Genes, p16 Amino Acid Substitution Virulence Genes, Duplicate Promoter Regions, Genetic Genes, erbB-2 Markov Chains Interphase Plasmids

Disciplines and Occupations4

Genomics Cytogenetics Immunohistochemistry Computational Biology

Information Science8

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

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 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 Chromosomes, Human, Pair 20 Cytogenetic Analysis In Situ Hybridization Mutation Chromosomes, Human, Pair 1 Gene Expression Profiling Cytogenetics Sequence Analysis, DNA Chromosomes, Human, Pair 8 Point Mutation Chromosome Disorders Genome, Bacterial Gene Deletion Base Sequence Molecular Sequence Data Polymerase Chain Reaction Mutation, Missense Chromosomes, Human, Pair 3 Chromosome Banding Intellectual Disability Genomic Instability Loss of Heterozygosity Chromosomes, Human, Pair 17 Chromosome Duplication Genome Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 9 Gene Duplication Spectral Karyotyping Phylogeny Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 6 Genetic Variation Chromosomes, Human, Pair 7 Microarray Analysis Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 12 Phenotype Chromosomes, Human, Pair 16 Abnormalities, Multiple Cluster Analysis Allelic Imbalance Chromosome Breakpoints Chromosomes, Human, Pair 15 Sequence Deletion Chromosomes, Human, Pair 2 Paraffin Embedding Polar Bodies Chromosomes, Human, Pair 22 DNA Microsatellite Repeats Chromosome Painting Gene Expression Regulation, Neoplastic Chromosome Breakage Pedigree Germ-Line Mutation DNA Mutational Analysis Segmental Duplications, Genomic Evolution, Molecular Chromosomal Instability Genes, Neoplasm Nucleic Acid Amplification Techniques Chromosomes, Human, Pair 18 Karyotype DNA, Bacterial Genomic Islands Translocation, Genetic Ploidies Preimplantation Diagnosis Genetic Testing Species Specificity Breast Neoplasms Chromosomes, Human, Pair 5 Exons Models, Genetic Genotype Chromosomes, Human, X Frameshift Mutation Chromosomes, Human, Pair 14 Amino Acid Sequence Cell Line, Tumor Multigene Family Prognosis

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