Thursday, October 6, 2011

Molecular Diagnosis of Genetic Diseases

Molecular Diagnosis of Genetic Diseases



Author:
Edition: 1st
Publisher: Humana Press
Binding: Plastic Comb
ISBN: 0896033465



Molecular Diagnosis of Genetic Diseases (Methods in Molecular Medicine)


Expert clinical investigators present their best and most reliable methods for the molecular diagnosis of common genetic disorders. Medical books Molecular Diagnosis of Genetic Diseases . Medical books Molecular Diagnosis of Genetic Diseases .... Molecular Diagnosis of Genetic Diseases Humana Press 9781617372599 09781617372599

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Molecular Diagnosis of Genetic Diseases Humana Press 9781617372599 09781617372599

Molecular Diagnosis of Genetic Diseases, ISBN-13: 9780896033467, ISBN-10: 0896033465

Electronics Cameras Computers Software Housewares Sports DVDs Music Books Games Toys in titles descriptions Company Info |Checkout Info |Shipping Info |Return Policy |FAQ's Add us as a favorite seller By continuing with your purchase using the eBay Buy It Now button, you agree to the Buy Terms of Use at http://stores.ebay.com/Buys-Internet-Superstore/Terms.html . Molecular Diagnosis of Genetic Diseases: Second Edition - Elles, Rob (EDT)/ Mountford, Roger (EDT)THIS IS A BRAND NEW UNOPENED ITEM.

Store Search search Title, ISBN and Author Molecular Diagnosis of Genetic Diseases Estimated delivery 3-12 business days Format Paperback Condition Brand New This completely revised and updated second edition to integrates the many new technologies and insights now available for the diagnosis of genetic diseases. The authors use such methodologies as PCR optimization dosage analysis, mutation scanning, and quantitative fluorescent PCR for aneuploidy analysis, Neurofibromatosis type 1, and Duche



Medical Book Molecular Diagnosis of Genetic Diseases



The methods-organized by disease or diagnostic area-are robust and reproducible. They contain not only essential day-to-day benchtop wisdom and instruction, but also offer possibilities for introducing new molecular genetic diagnostic tests, as well as invaluable advice on controls, quality standards, and interpretation. Among the genetic diseases discussed are Duchenne/Becker muscular dystrophy, familial adenomatous polyposis, X-chromosome inactivation, Prader-Willi and Angelman syndromes, Huntington's disease, myotonic dystrophy, fragile X disease, cystic fibrosis, familial hypochloresterolemia, and the hemoglobinopathies.

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