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Genodermatoses: A Full Color Clinical Guide to Genetic Skin Disorders
Hardback

Genodermatoses: A Full Color Clinical Guide to Genetic Skin Disorders

$404.00
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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. Features: - 20-30% new material – update genetic mutations, pathogenesis,
prognosis, clinical pearls, management - Add 5 new entities - Update clinical photos under line drawings (~ 20% new) - Boxed features highlight clinical pearls and add insight and breadth
to the material - Bulleted text summarizing the patterns of inheritance, prenatal
diagnosis, incidence, age of presentation, pathogenesis, key features,
differential diagnosis, laboratory findings, management, and prognosis - 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

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MORE INFO
Format
Hardback
Publisher
Lippincott Williams and Wilkins
Country
United States
Date
1 March 2024
Pages
448
ISBN
9781451116519

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. Features: - 20-30% new material – update genetic mutations, pathogenesis,
prognosis, clinical pearls, management - Add 5 new entities - Update clinical photos under line drawings (~ 20% new) - Boxed features highlight clinical pearls and add insight and breadth
to the material - Bulleted text summarizing the patterns of inheritance, prenatal
diagnosis, incidence, age of presentation, pathogenesis, key features,
differential diagnosis, laboratory findings, management, and prognosis - 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

Read More
Format
Hardback
Publisher
Lippincott Williams and Wilkins
Country
United States
Date
1 March 2024
Pages
448
ISBN
9781451116519