ISCN 2013: An International System for Human Cytogenetic Nomenclature (2013) Published in Collaboration with 'Cytogenetic and Genome Research'

ISCN 2013: An International System for Human Cytogenetic Nomenclature (2013) Published in Collaboration with 'Cytogenetic and Genome Research'

Paperback

Edited by L.G. Shaffer, Edited by Jean McGowan-Jordan, Edited by M. Schmid

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  • Publisher: S Karger Ag
  • Format: Paperback | 140 pages
  • Dimensions: 174mm x 250mm x 8mm | 621g
  • Publication date: 1 December 2012
  • Publication City/Country: Basel
  • ISBN 10: 3318022535
  • ISBN 13: 9783318022537
  • Edition: 1
  • Illustrations note: 11, in Color: Tables:4
  • Sales rank: 107,086

Product description

This publication extends the now classic system of human cytogenetic nomenclature prepared by an expert committee and published in collaboration with 'Cytogenetic and Genome Research' since 1963. Revised and finalized by the ISCN Committee and its advisors at a meeting in Seattle, Wash., in April 2012, the "ISCN 2013" updates, revises and incorporates all previous human cytogenetic nomenclature recommendations into one systematically organized publication that supersedes all previous ISCN recommendations. There are several new features in "ISCN 2013": an update of the microarray nomenclature, many more illustrative examples of uses of nomenclature in all sections; some definitions including chromothripsis and duplication; and, a new chapter for nomenclature that can be used for any region-specific assay. "The ISCN 2013" is an indispensable reference volume for human cytogeneticists, technicians and students for the interpretation and communication of human cytogenetic nomenclature.

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Table of 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; Microarrays; Region-Specific Assays.