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ISCN : an international system for human cytogenomic nomenclature (2016) / editors, Jean McGowan-Jordan, Ottawa, Ont., Annet Simons, Nijmegen, Michael Schmid, Würzburg.

By: Contributor(s): Material type: TextTextPublisher: Basel ; New York : Karger, 2016Description: vi, 139 p. : il. ; 28 cmISBN:
  • 9783318058574
Other title:
  • International system for human cytogenomic nomenclature (2016)
Uniform titles:
  • Contained in (work): Cytogenetic and genome research.
Subject(s):
Contents:
Historical introduction -- Normal chromosomes -- Symbols and abbreviated terms -- Karyotype designation -- Uncertainty in chromosome or band designation -- Order of chromosome abnormalities in the karyotype -- Normal variable chromosome features -- Numerical chromosome abnormalities -- Structural chromosome rearrangements -- Chromosome breakage -- Neoplasia -- Meiotic chromosomes -- In situ hybridization -- Miicroarrays -- Region-speciifc assays -- Sequence-based assays.
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Item type Home library Call number Status Barcode
Books Books Centro de Información Eduardo Savino Revistero 575.1 (083.72) ISCN (Browse shelf(Opens below)) Available 51398
Total holds: 0

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543: 519.237.7 M251 Factor analysis in chemistry / 544.034: 517.95 V979 Diffusion and mass transfer / 556.114.6: 54.027 F396 Isotopes of the earth's hydrosphere / 575.1 (083.72) ISCN ISCN : 575.11/.13: 54.06 M214 Cytogenetic laboratory management : 612.014.48 H141 7ed. Radiobiology for the radiologist / 620.179.1 M425 Materials characterization using nondestructive evaluation (NDE) methods /

"Recommendations of the International Standing Committee on Human Cytogenomic Nomenclature, including new sequence-based cytogenomic nomenclature developed in collaboration with the Human Genome Variation Society (HGVS) Sequence Variant Description Working Group."

Publicado en Cytogenetic and Genome Research vol. 149, no. 1-2 (2016) bajo el título ISCN 2016: An International System for Human Cytogenomic Nomenclature.

Incluye referencias bibliográficas e índice analítico.

Historical introduction -- Normal chromosomes -- Symbols and abbreviated terms -- Karyotype designation -- Uncertainty in chromosome or band designation -- Order of chromosome abnormalities in the karyotype -- Normal variable chromosome features -- Numerical chromosome abnormalities -- Structural chromosome rearrangements -- Chromosome breakage -- Neoplasia -- Meiotic chromosomes -- In situ hybridization -- Miicroarrays -- Region-speciifc assays -- Sequence-based assays.

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