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Ladataan... Genodermatoses: A Clinical Guide to Genetic Skin Disorders (vuoden 2004 painos)4 | - | 2,785,377 | - | - | 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.… (lisätietoja) |
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Alkuperäinen julkaisuvuosi |
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Henkilöt/hahmot |
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Kirjaan liittyvät elokuvat |
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Palkinnot ja kunnianosoitukset |
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Epigrafi (motto tai mietelause kirjan alussa) |
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Omistuskirjoitus |
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Ensimmäiset sanat |
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Sitaatit |
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Viimeiset sanat |
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Alkuteoksen kieli |
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Canonical DDC/MDS |
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▾Viitteet Viittaukset tähän teokseen muissa lähteissä. Englanninkielinen Wikipedia (1)
▾Kirjojen kuvailuja 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. ▾Kirjastojen kuvailut No library descriptions found. ▾LibraryThingin jäsenten laatimat kuvailut
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