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Cytogenetic abnormalities : chromosomal, FISH, and microarray-based clinical reporting / Susan Mahler Zneimer, CEO and Scientific Director, MOSYS Consulting, Adjunct Professor, Moorpark College, Moorpark, California.

By: Material type: TextTextPublication details: Chichester, West Sussex : Wiley-Blackwell, c2014.Edition: 1st edDescription: xiii, 647 p. : illustrations ; 26 cmISBN:
  • 9781118912492 (paperback)
  • 1118912497 (paperback)
  • 9781118412558 (cloth)
  • 1118412559 (cloth)
Subject(s): Additional physical formats: Online version:: Cytogenetic abnormalitiesDDC classification:
  • 572.8/7 23 ZNE-C
LOC classification:
  • QH600 .Z64 2014
  • RB155.5 .Z54 2014
NLM classification:
  • QS 677
Summary: "This guide discusses chromosomal abnormalities and how best to report and communicate lab findings in research and clinical settings. Providing a standard approach to writing cytogenetic laboratory reports, the guide further covers useful guidance on implementing International System for Human Cytogenetic Nomenclature in reports. Part one of the guide explores chromosomal, FISH, and microarray analysis in constitutional cytogenetic analyses, while part two looks at acquired abnormalities in cancers. Both sections provide illustrative examples of chromosomal abnormalities and how to communicate these findings in standardized laboratory reports"--
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Holdings
Item type Current library Home library Call number Status Date due Barcode
Book Book IUCEIB Library, University of Kerala General Stacks IUCEIB Library, University of Kerala 572.87 ZNE.C (Browse shelf(Opens below)) Available CEB606

Includes bibliographical references and index.

"This guide discusses chromosomal abnormalities and how best to report and communicate lab findings in research and clinical settings. Providing a standard approach to writing cytogenetic laboratory reports, the guide further covers useful guidance on implementing International System for Human Cytogenetic Nomenclature in reports. Part one of the guide explores chromosomal, FISH, and microarray analysis in constitutional cytogenetic analyses, while part two looks at acquired abnormalities in cancers. Both sections provide illustrative examples of chromosomal abnormalities and how to communicate these findings in standardized laboratory reports"--

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