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Copy number abnormality

См. также в других словарях:

  • Chromosome abnormality — The three major single chromosome mutations; deletion (1), duplication (2) and inversion (3) …   Wikipedia

  • Aneuploidy — Classification and external resources ICD 10 Q90 Q98 ICD 9 …   Wikipedia

  • Autism — This article is about the classic autistic disorder; some writers use the word autism when referring to the range of disorders on the autism spectrum or to the various pervasive developmental disorders.[1] Autism …   Wikipedia

  • Chromosome — For a non technical introduction to the topic, see Introduction to genetics. Diagram of a replicated and condensed metaphase eukaryotic chromosome. (1) Chromatid – one of the two identical parts of the chromosome after S phase. (2)… …   Wikipedia

  • B-cell chronic lymphocytic leukemia — B cell CLL redirects here. For the gene family, see B cell CLL/lymphoma. Chronic lymphocytic leukemia Classification and external resources Peripheral blood smear showing CLL cells ICD 10 …   Wikipedia

  • Causes of schizophrenia — Schizophrenia is a psychiatric diagnosis that describes a mental disorder characterized by impairments in the perception or expression of reality and by significant social or occupational dysfunction. A person experiencing schizophrenia is… …   Wikipedia

  • Multiple myeloma — Classification and external resources Micrograph of a plasmacytoma, the histologic correlate of multiple myeloma. H E stain ICD …   Wikipedia

  • Karyotype — A karyotype is the number and appearance of chromosomes in the nucleus of an eukaryotic cell. The term is also used for the complete set of chromosomes in a species, or an individual organism.[1][2]p28[3] Karyotypes describe the number of… …   Wikipedia

  • Schizophrenia — MeshName = Schizophrenia MeshNumber = F03.700.750 Schizophrenia (pron en|ˌskɪtsəˈfriːniə), from the Greek roots schizein (σχίζειν, to split ) and phrēn , phren (φρήν, φρεν , mind ) is a psychiatric diagnosis that describes a mental disorder… …   Wikipedia

  • Chromosomal translocation — of the 4th and 20th chromosome. In genetics, a chromosome translocation is a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes. A gene fusion may be created when the translocation joins two otherwise… …   Wikipedia

  • genetic disease, human — Introduction       any of the diseases and disorders that are caused by mutations in one or more genes (gene).       With the increasing ability to control infectious and nutritional diseases in developed countries, there has come the realization …   Universalium

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