Genodermatoses: A Clinical Guide to Genetic Skin Disorders

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9780781740883: Genodermatoses: A Clinical Guide to Genetic Skin Disorders

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.

"Sinopsis" puede pertenecer a otra edición de este libro.

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Spitz, Joel L.
ISBN 10: 0781740886 ISBN 13: 9780781740883
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Descripción 2004. HRD. Estado de conservación: New. New Book. Shipped from US within 10 to 14 business days. Established seller since 2000. Nº de ref. de la librería T2-9780781740883

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Joel L. Spitz (Editor)
Editorial: Lippincott Williams & Wilkins (2004)
ISBN 10: 0781740886 ISBN 13: 9780781740883
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Descripción Lippincott Williams & Wilkins, 2004. Hardcover. Estado de conservación: New. Second. Nº de ref. de la librería DADAX0781740886

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Editorial: Lippincott Williams and Wilkins, United States (2004)
ISBN 10: 0781740886 ISBN 13: 9780781740883
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Descripción Lippincott Williams and Wilkins, United States, 2004. Hardback. Estado de conservación: New. 2nd edition. Language: English . Brand New Book. 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-glanceFull body diagrams and clinical photographs of each syndromeBulleted text summarizing the patterns of inheritance, prenatal diagnosis, incidence, age of presentation, pathogenesis, key features, differential diagnosis, laboratory findings, management, and prognosisBoxed features highlight clinical pearls and add insight and breadth to the materialNew 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. Nº de ref. de la librería AAS9780781740883

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Editorial: Lippincott Williams and Wilkins, United States (2004)
ISBN 10: 0781740886 ISBN 13: 9780781740883
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The Book Depository US
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Descripción Lippincott Williams and Wilkins, United States, 2004. Hardback. Estado de conservación: New. 2nd edition. Language: English . Brand New Book. 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-glanceFull body diagrams and clinical photographs of each syndromeBulleted text summarizing the patterns of inheritance, prenatal diagnosis, incidence, age of presentation, pathogenesis, key features, differential diagnosis, laboratory findings, management, and prognosisBoxed features highlight clinical pearls and add insight and breadth to the materialNew syndromes such as PHACE, AEC, EEC, Griscelli, and Birt-Hogg-DubeAs 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. Nº de ref. de la librería AAS9780781740883

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Joel L. Spitz (editor)
Editorial: LWW 2004-12-29, Philadelphia, Pa. |London (2004)
ISBN 10: 0781740886 ISBN 13: 9780781740883
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Blackwell's
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Descripción LWW 2004-12-29, Philadelphia, Pa. |London, 2004. hardback. Estado de conservación: New. Nº de ref. de la librería 9780781740883

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Editorial: Lippincott Williams and Wilkins, United States (2004)
ISBN 10: 0781740886 ISBN 13: 9780781740883
Nuevos Tapa dura Cantidad: 10
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Book Depository hard to find
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Descripción Lippincott Williams and Wilkins, United States, 2004. Hardback. Estado de conservación: New. 2nd edition. Language: English . This book usually ship within 10-15 business days and we will endeavor to dispatch orders quicker than this where possible. Brand New Book. 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-glanceFull body diagrams and clinical photographs of each syndromeBulleted text summarizing the patterns of inheritance, prenatal diagnosis, incidence, age of presentation, pathogenesis, key features, differential diagnosis, laboratory findings, management, and prognosisBoxed features highlight clinical pearls and add insight and breadth to the materialNew syndromes such as PHACE, AEC, EEC, Griscelli, and Birt-Hogg-DubeAs 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. Nº de ref. de la librería BZE9780781740883

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Editorial: LWW
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Descripción LWW. Hardcover. Estado de conservación: New. 0781740886 New. Looks like an interesting title, learn more! We provide domestic tracking upon request. We provide personalized customer service and want you to have a great experience purchasing from us. 100% satisfaction guaranteed and thank you for your consideration. Nº de ref. de la librería S-0781740886

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Editorial: LWW (2004)
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Descripción LWW, 2004. Hardcover. Estado de conservación: New. Nº de ref. de la librería P110781740886

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Spitz, Joel L./ Hatch, Vaune J. (Illustrator)/ Spitz, Joel L. (Editor)
Editorial: Lippincott Williams & Wilkins (2004)
ISBN 10: 0781740886 ISBN 13: 9780781740883
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Descripción Lippincott Williams & Wilkins, 2004. Hardcover. Estado de conservación: Brand New. 2nd edition. 424 pages. 11.00x8.75x1.00 inches. In Stock. Nº de ref. de la librería z-0781740886

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Editorial: Lippincott Williams and Wilkins (2004)
ISBN 10: 0781740886 ISBN 13: 9780781740883
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Descripción Lippincott Williams and Wilkins, 2004. Estado de conservación: New. Nº de ref. de la librería TH9780781740883

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