Specially designed for dermatologists, pediatricians, and family physicians, this user-friendly guide to genetic skin disorders is an ideal resource for both board preparation and clinical practice. To help make learning a difficult subject more efficient and effective, the text takes a user-friendly, visual approach, featuring more than 300 full-color illustrations and a format designed for maximum retention of content. You’ll find features like these– / Each syndrome is presented in easy-to-read, two-page spreads, allowing you to read material in depth or at-a-glance / Full body diagrams and clinical photographs of each syndrome / Bulleted text summarizing the patterns of inheritance, prenatal diagnosis, incidence, age of presentation, pathogenesis, key features, differential diagnosis, laboratory findings, management, and prognosis / Boxed features highlight clinical pearls and add insight and breadth to the material / New syndromes such as PHACE, AEC, EEC, Griscelli, and Birt-Hogg-Dube As a board preparation tool or on-the-job resource, this powerful reference is valued for its breadth and depth as well as its compact, efficient format.

Genodermatoses A Clinical Guide to Genetic Skin Disorders

Product Details

  • Hardcover: 424 pages
  • Publisher: Lippincott Williams & Wilkins; Second Edition edition (December 1, 2004)
  • Language: English
  • ISBN-10: 0781740886
  • ISBN-13: 978-0781740883.

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Genodermatoses A Clinical Guide to Genetic Skin Disorders

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