Smith's Recognizable Patterns Of Human Malformation Sixth Edition 在线电子书 pdf 下载 txt下载 epub 下载 mobi 下载 2024


Smith's Recognizable Patterns Of Human Malformation Sixth Edition

简体网页||繁体网页
Jones MD, Kenneth Lyons 作者
Elsevier Science Health Science div
译者
2005-8 出版日期
976 页数
881.00元 价格
HRD
丛书系列
9780721606156 图书编码

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发表于2024-07-05


Smith's Recognizable Patterns Of Human Malformation Sixth Edition 在线电子书 epub 下载 mobi 下载 pdf 下载 txt 下载 2024

Smith's Recognizable Patterns Of Human Malformation Sixth Edition 在线电子书 epub 下载 mobi 下载 pdf 下载 txt 下载 2024

Smith's Recognizable Patterns Of Human Malformation Sixth Edition 在线电子书 pdf 下载 txt下载 epub 下载 mobi 下载 2024



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Smith's Recognizable Patterns Of Human Malformation Sixth Edition 在线电子书 pdf 下载 txt下载 epub 下载 mobi 在线电子书下载

Smith's Recognizable Patterns Of Human Malformation Sixth Edition 在线电子书 图书描述

The completely revised and updated New Edition of this definitive text—now in full color! Long known as the source to consult for guidance on diagnosis, prognosis, plan management, and genetic counseling, this easy-to-use reference focuses on the patterns of human defects caused by inborn errors in morphogenesis as opposed to defects caused by mechanical problems. It provides a wealth of information on normal and abnormal morphogenesis * minor anomalies and their relevance * clinical approaches to specific diagnoses * and normal standards of measurement for the entire spectrum of disorders. Each chapter includes a description of the specific abnormality—including occasional associated abnormalities—natural history, etiology, and references. On opposing pages are several descriptive photographs and line drawings of either an individual with the abnormality or specific features of the abnormality. * Provides over 1,450 photographs and illustrations to depict each malformation—many from the personal collections of Drs. Smith and Jones—to aid readers in diagnosis. * Uses a consistent chapter format to help readers quickly and easily find information on any given disorder * Offers the most current coverage available on existing disorders and their molecular basis, plus the very latest information on virtually any genetic or physiological malformation.

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