Methods in Molecular Medicine Vol.5 Molecular Diagnosis of Genetic Diseases

Discussion in 'Methods in Molecular Medicine Book Series' started by sangtranhm, May 7, 2016.

  1. sangtranhm

    sangtranhm New Member

    Expert clinical investigators present their best and most reliable methods for the molecular diagnosis of common genetic disorders. 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.
    • Series: Methods in Molecular Medicine (Book 5)
    • Paperback: 372 pages
    • Publisher: Humana Press; 1 edition (July 19, 1996)
    • Language: English
    • ISBN-10: 0896033465
    • ISBN-13: 978-0896033467
    • Product Dimensions: 9 x 6.4 x 1.1 inches
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    Last edited by a moderator: Nov 14, 2021

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