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Titlebook: Genetic Disorders and the Fetus; Diagnosis, Preventio Aubrey Milunsky (Assistant Professor, Director, Me Book 1979 Aubrey Milunsky 1979 Lab

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發(fā)表于 2025-3-21 20:05:54 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Genetic Disorders and the Fetus
副標(biāo)題Diagnosis, Preventio
編輯Aubrey Milunsky (Assistant Professor, Director, Me
視頻videohttp://file.papertrans.cn/383/382480/382480.mp4
圖書封面Titlebook: Genetic Disorders and the Fetus; Diagnosis, Preventio Aubrey Milunsky (Assistant Professor, Director, Me Book 1979 Aubrey Milunsky 1979 Lab
描述Technological advances continue to expand the number of genetic disorders that can be diagnosed in utero. Utilization of this new technology has de- manded special expertise available in relatively few academic centers. As these new applications have become more widespread so have the realities of the medicolegal implications. Notwithstanding the laboratory challenges, most legal action, at least in the United States, has arisen from the physician‘s failure to inform a patient about the risks of a genetic disorder or the oppor- tunities presented by prenatal diagnosis. Hence an extensive thorough reex- amination of the subject seems appropriate and timely. The steady escalation in the number of prenatal genetic studies now being done in the western world makes it imperative for the physician to have a thorough comprehension of the subject in its entirety. I am, therefore, fortu- nate in having colleagues who as acknowledged experts have shared their knowledge and experience in order to make this volume a major critical repository of facts and guidance about prenatal genetic diagnosis. The subject matter ranges from a consideration of required genetic counseling through the intricac
出版日期Book 1979
關(guān)鍵詞Laboratory; Termination; Xeroderma pigmentosum; attention; chromosome; counseling; development; diagnosis; e
版次1
doihttps://doi.org/10.1007/978-1-4684-3438-5
isbn_softcover978-1-4684-3440-8
isbn_ebook978-1-4684-3438-5
copyrightAubrey Milunsky 1979
The information of publication is updating

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The Shelleys and Dante’s Matildaeuploidies (Pai et al., 1978) suggests possible infectious causes. Indeed, if vertically transmitted RNA retroviruses exist in the germ plasm of humans, as they do in other species, such chromosomally integrated viral genetic material might well affect embryogenesis (Temin, 1976). Furthermore, the p
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- nate in having colleagues who as acknowledged experts have shared their knowledge and experience in order to make this volume a major critical repository of facts and guidance about prenatal genetic diagnosis. The subject matter ranges from a consideration of required genetic counseling through the intricac978-1-4684-3440-8978-1-4684-3438-5
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Amniotic Fluid Cell Culture,961; Parmley and Miller, 1969). It is just possible that this evidence of keratinization prior to 20 weeks of pregnancy may ultimately lead to the prenatal detection of hereditary disorders of keratin, such as the ichthyoses (Goodman, 1970).
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