Molecular Diagnostics, Second Edition |  | Creators: George Patrinos, Wilhelm Ansorge Publisher: Academic Press
List Price: $129.95 Buy New: $103.96 as of 11/22/2009 22:01 CST details You Save: $25.99 (20%)
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Seller: Amazon.com Sales Rank: 1222475
Media: Hardcover Edition: 2 Pages: 598 Number Of Items: 1 Shipping Weight (lbs): 4 Dimensions (in): 11 x 8.6 x 1.1
ISBN: 0123745373 Dewey Decimal Number: 616 EAN: 9780123745378 ASIN: 0123745373
Publication Date: October 7, 2009 Shipping: Eligible for FREE Super Saver Shipping Availability: Usually ships in 24 hours
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Product Description Key Features . Contains state-of-the-art techniques for the detection of the underlying genetic heterogeneity leading to inherited disorders . Includes in-depth discussion of ethical and safety considerations . Identifies genetically modified organisms (GMO's) . Covers forensic analysis and every-day issues in a diagnostic laboratory
Description The second edition of Molecular Diagnostics, the only book dealing with diagnosis on a molecular level, discusses current molecular biological techniques used to identify the underlying molecular defects in inherited disease. The book delves further into the principle and brief description of the technique, followed by examples from the authors' own expertise. Contributors to the 2/e are well-known experts in their field, and derive from a variety of disciplines, to ensure breadth and depth of coverage. Molecular Diagnostics, 2/e , is a needed resource for graduate students, researchers, physicians and practicing scientists in molecular genetics; professionals from similar backgrounds working in diagnostic laboratories in academia or industry, as well as, academic institutions and hospital libraries.
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Key Features: *Deals exclusively with the currently used molecular biology techniques to identify the underlying molecular defect of inherited diseases
*Includes pharmacogenetics and pharmacogenomics relating to new cancer therapies
*Provies a comprehensive guide through emerging concepts and demonstrates how the available mutation screening technology can be implemented in diagnostic laboratories and provide better healthcare
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