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Titlebook: Lynch Syndrome; Molecular Mechanism Naohiro Tomita Book 2020 Springer Nature Singapore Pte Ltd. 2020 Colorectal cancer.Colorectal neoplasm

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書目名稱Lynch Syndrome
副標(biāo)題Molecular Mechanism
編輯Naohiro Tomita
視頻videohttp://file.papertrans.cn/590/589234/589234.mp4
概述Provides a comprehensive review of Lynch syndrome.Offers essential insights into a new phase in the management of Lynch syndrome.Describes the genetic and epigenetic basis of Lynch syndrome
圖書封面Titlebook: Lynch Syndrome; Molecular Mechanism  Naohiro Tomita Book 2020 Springer Nature Singapore Pte Ltd. 2020 Colorectal cancer.Colorectal neoplasm
描述.This book offers a comprehensive review of Lynch Syndrome (LS), addressing both the basic and clinical aspects of this condition...Due to the recent advances in our understanding of the genetic mechanism of LS, and to new screening methods, including universal screening and/or multi-gene panel analysis, the standard treatment strategy for patients and family members of LS have been steadily improving. In this book, experts describe the disease’s manifestations, discuss state-of-the-art diagnosis and management options, and offer a cutting-edge overview of the genetic and epigenetic basis of the syndrome...Providing essential insights into this new phase in the management of LS, this book is a valuable resource not only for colorectal surgeons, but also for general gastrointestinal clinicians, gynecologists, oncologists and all basic researchers with an interest in LS..
出版日期Book 2020
關(guān)鍵詞Colorectal cancer; Colorectal neoplasms; Gynecological malignancies; Urological malignancies; Multiple-g
版次1
doihttps://doi.org/10.1007/978-981-15-6891-6
isbn_softcover978-981-15-6893-0
isbn_ebook978-981-15-6891-6
copyrightSpringer Nature Singapore Pte Ltd. 2020
The information of publication is updating

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International Collaboration for Lynch Syndrome,lished in 2005. This society was always the center of the physician, surgeon, researcher, geneticist, genetic counselor, etc. involved in this field and established clinical criteria and central database with collection of causative gene alterations for clinical use. It also supported multiple inter
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