Chromosomal instability aneuploidy. Medical search. Frequent questions

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Anatomy40

Centrosome Chromosomes, Human Telomere Chromosomes Spindle Apparatus Micronuclei, Chromosome-Defective Chromosomes, Human, Pair 18 Centromere Kinetochores Fibroblasts Cell Line, Tumor Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 7 Spermatozoa Cell Line Microtubules Polar Bodies Chromosomes, Human, X Lymphocytes Chromosomes, Human, Pair 13 Cells, Cultured Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 20 Embryo, Mammalian Sex Chromosomes Chromosomes, Human, Y Tumor Cells, Cultured Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 1 Cell Nucleus Chromosomes, Human, Pair 21 Chromosomes, Human, Pair 9 Y Chromosome Hybrid Cells Cell Line, Transformed HCT116 Cells HeLa Cells Chromatids Oocytes Epithelial Cells

Organisms4

Cricetinae Mice, Knockout JC Virus Mice, Transgenic

Diseases44

Chromosomal Instability Aneuploidy Genomic Instability Chromosome Aberrations Joint Instability Microsatellite Instability Polyploidy Chromosome Breakage Chromosome Disorders Chromosome Fragility Cell Transformation, Neoplastic Fanconi Anemia Nijmegen Breakage Syndrome Micronuclei, Chromosome-Defective Colorectal Neoplasms Neoplasms Bloom Syndrome Trisomy Ataxia Telangiectasia Translocation, Genetic Abnormal Karyotype Tetraploidy Nondisjunction, Genetic Microcephaly Precancerous Conditions Down Syndrome Colonic Neoplasms Chromosome Deletion Infertility, Male Gonadal Disorders Breast Neoplasms Gonadal Dysgenesis, 46,XX Adenoma XYY Karyotype Sex Chromosome Aberrations Adenocarcinoma Klinefelter Syndrome Syndrome Disease Progression Lymphoma Oligospermia Carcinoma Abortion, Spontaneous Genetic Predisposition to Disease

Chemicals and Drugs47

Cell Cycle Proteins Mad2 Proteins Aurora Kinase A DNA, Neoplasm Aurora Kinases Protein-Serine-Threonine Kinases Nuclear Proteins Tumor Suppressor Protein p53 Telomerase DNA-Binding Proteins Fanconi Anemia Complementation Group G Protein Fanconi Anemia Complementation Group Proteins RecQ Helicases Nocodazole DNA Mitomycin Aneugens Ataxia Telangiectasia Mutated Proteins Securin Neoplasm Proteins Fanconi Anemia Complementation Group C Protein Fanconi Anemia Complementation Group A Protein Antigens, Nuclear Hypoxanthine Phosphoribosyltransferase F-Box Proteins Fanconi Anemia Complementation Group F Protein Tumor Suppressor Proteins Rad51 Recombinase DNA Helicases Chromosomal Proteins, Non-Histone Cyclin B1 Cyclin B Mutagens BRCA2 Protein DNA Repair Enzymes Adenomatous Polyposis Coli Protein Telomeric Repeat Binding Protein 1 Fanconi Anemia Complementation Group D2 Protein MutS Homolog 2 Protein Adaptor Proteins, Signal Transducing Telomeric Repeat Binding Protein 2 Histones Repressor Proteins Cyclin E Proto-Oncogene Proteins RNA, Small Interfering DNA, Satellite

Analytical, Diagnostic and Therapeutic Techniques and Equipment29

In Situ Hybridization, Fluorescence Karyotyping Cytogenetic Analysis Spectral Karyotyping Preimplantation Diagnosis Micronucleus Tests Comparative Genomic Hybridization Flow Cytometry Nucleic Acid Hybridization Models, Biological Polymerase Chain Reaction Chromosome Banding Prognosis Models, Genetic Mitotic Index Prenatal Diagnosis Reverse Transcriptase Polymerase Chain Reaction Oligonucleotide Array Sequence Analysis Immunohistochemistry Gene Expression Profiling Primed In Situ Labeling DNA Mutational Analysis Blotting, Western Maternal Serum Screening Tests Sperm Injections, Intracytoplasmic Genetic Testing Chromosome Mapping Ultrasonography, Prenatal Microscopy, Fluorescence

Phenomena and Processes103

Chromosomal Instability Aneuploidy Genomic Instability Chromosome Aberrations Microsatellite Instability Chromosome Segregation Ploidies Mitosis Polyploidy Chromosome Breakage Chromosomes, Human Telomere Chromosome Fragility Diploidy Chromosomes DNA Damage Microsatellite Repeats DNA Repair Loss of Heterozygosity Mutation Mosaicism Micronuclei, Chromosome-Defective Chromosomes, Human, Pair 18 Metaphase Sister Chromatid Exchange Centromere Kinetochores M Phase Cell Cycle Checkpoints Trisomy Chromosome Fragile Sites Gene Dosage Phenotype Cytokinesis Anaphase Cell Cycle Translocation, Genetic Abnormal Karyotype Chromosomes, Human, Pair 17 Tetraploidy Telomere Shortening DNA Methylation Chromosomes, Human, Pair 7 Nondisjunction, Genetic Meiosis Radiation, Ionizing DNA Breaks, Double-Stranded Recombination, Genetic Genes, p53 Gene Amplification Chromosomes, Human, X Genes, cdc Karyotype Nucleic Acid Hybridization DNA Replication Gene Deletion Allelic Imbalance Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 4 Cell Aging Chromosomes, Human, Pair 20 Gene Expression Regulation, Neoplastic X-Rays Pregnancy Sex Chromosomes Chromosomes, Human, Y Chromosomes, Human, Pair 8 Chromosome Deletion Chromosomes, Human, Pair 1 Maternal Age Cell Division Chromosomes, Human, Pair 21 Bystander Effect Chromosomes, Human, Pair 9 G2 Phase Gene Rearrangement XYY Karyotype Sex Chromosome Aberrations Radiation Tolerance Base Sequence Heterozygote Y Chromosome Genes, ras Apoptosis Gamma Rays Time Factors CpG Islands Alleles Epigenesis, Genetic Genes, Tumor Suppressor Chromatids S Phase Cell Proliferation Cell Survival DNA Sequence, Unstable Genome RNA Interference DNA, Satellite Pregnancy Trimester, First Mutagenesis Genes, APC Gene Silencing Genetic Predisposition to Disease Sequence Deletion

Disciplines and Occupations2

Immunohistochemistry Cytogenetics

Information Science2

Base Sequence Molecular Sequence Data

Health Care2

Maternal Age Genetic Testing

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

Chromosomal Instability Aneuploidy Genomic Instability Chromosome Aberrations In Situ Hybridization, Fluorescence Joint Instability Karyotyping Microsatellite Instability Chromosome Segregation Centrosome Ploidies Mitosis Polyploidy Chromosome Breakage Chromosomes, Human Telomere Chromosome Disorders Chromosome Fragility Diploidy Chromosomes DNA Damage Cell Cycle Proteins Mad2 Proteins Aurora Kinase A Cell Transformation, Neoplastic Microsatellite Repeats Spindle Apparatus DNA, Neoplasm Aurora Kinases Fanconi Anemia DNA Repair Loss of Heterozygosity Mutation Mosaicism Nijmegen Breakage Syndrome Cytogenetic Analysis Micronuclei, Chromosome-Defective Spectral Karyotyping Protein-Serine-Threonine Kinases Chromosomes, Human, Pair 18 Metaphase Colorectal Neoplasms Preimplantation Diagnosis Neoplasms Sister Chromatid Exchange Nuclear Proteins Tumor Suppressor Protein p53 Centromere Bloom Syndrome Kinetochores M Phase Cell Cycle Checkpoints Trisomy Micronucleus Tests Chromosome Fragile Sites Telomerase DNA-Binding Proteins Comparative Genomic Hybridization Gene Dosage Phenotype Fibroblasts Ataxia Telangiectasia Cell Line, Tumor Cytokinesis Anaphase Cell Cycle Translocation, Genetic Abnormal Karyotype Chromosomes, Human, Pair 17 Fanconi Anemia Complementation Group G Protein Tetraploidy Telomere Shortening Fanconi Anemia Complementation Group Proteins RecQ Helicases DNA Methylation Chromosomes, Human, Pair 7 Nondisjunction, Genetic Spermatozoa Cell Line Meiosis Nocodazole Radiation, Ionizing DNA Breaks, Double-Stranded DNA Recombination, Genetic Flow Cytometry Genes, p53 Mitomycin Gene Amplification Aneugens Microtubules Ataxia Telangiectasia Mutated Proteins Securin Polar Bodies Chromosomes, Human, X Genes, cdc Microcephaly Precancerous Conditions Karyotype Nucleic Acid Hybridization Down Syndrome

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