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Titlebook: Genetic Disorders and the Fetus; Diagnosis, Preventio Aubrey Milunsky (Professor of Pediatrics, Obstetri Book 1986Latest edition Aubrey Mil

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發(fā)表于 2025-3-21 17:46:42 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Genetic Disorders and the Fetus
副標(biāo)題Diagnosis, Preventio
編輯Aubrey Milunsky (Professor of Pediatrics, Obstetri
視頻videohttp://file.papertrans.cn/383/382479/382479.mp4
圖書封面Titlebook: Genetic Disorders and the Fetus; Diagnosis, Preventio Aubrey Milunsky (Professor of Pediatrics, Obstetri Book 1986Latest edition Aubrey Mil
描述About 21 years ago prenatal diagnosis became part of the physician‘s diagnostic armamentarium against genetic defects. My first monograph in 1973 (The Prenatal Diagnosis of Hereditary Disorders) critically assessed early progress and enunciated basic principles in the systematic approach to prenatal genetic diagnosis. Six years later and under the current title, a subsequent volume provided the first major reference source on this subject. The present second (effectively third) edition, which was urged in view of the excellent reception of the two earlier volumes, reflects the remarkable growth of this new discipline and points to significant and exciting future developments. Notwithstanding these advances, the use of the new tools and techniques for the benefit of at-risk parents has taken many more years than most anticipated. Key factors have been the lack of teaching of human genetics in medical schools in the preceding decades and the difficulty of educating practicing physicians in a new scientific disci- pline. Even today the teaching of genetics in medical schools leaves much to be desired and this will further delay the introduction of newer genetic advances to the bedside
出版日期Book 1986Latest edition
關(guān)鍵詞anatomy; birth; child; complications; fetus; genetics; hormones; infection; placenta; pregnancy; prenatal diag
版次2
doihttps://doi.org/10.1007/978-1-4684-5155-9
isbn_softcover978-1-4684-5157-3
isbn_ebook978-1-4684-5155-9
copyrightAubrey Milunsky 1986
The information of publication is updating

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沙發(fā)
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It Goes Without Saying — But Not Alwaysal diagnosis, allowing increasingly accurate assessment of fetal physiology and metabolism. Since the amniotic fluid can be viewed as an extension of the fetal extracellular space (Lind et al., 1969; Lind and Hytten, 1970), an understanding of its origin, formation, and chemical constitution is cruc
地板
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Images of Dance in the Screen Media,(Milunsky, 1979), and the reader is encouraged to peruse that chapter along with the present one. Much valuable information deriving from the extensive personal experience of the author of that chapter (Milunsky, 1973, 1979) has remained accurate and timely, and thus will not be repeated here. This
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Dance, Consumerism, and Spiritualityination can be made by examination of the X-chromatin body in human amniotic fluid cells. A decade later, Steele and Breg (1966) succeeded in culturing amniotic fluid cells and karyotyping fetal chromosomes. This discovery advanced the role of genetic counseling for parents at risk of having a chrom
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發(fā)表于 2025-3-22 14:58:19 | 只看該作者
Ballet, Gender and Cultural Powerlly retarded institutionalized males than females. Although Martin and Bell (1943) and Renpenning et al. (1962) described families with characteristic X-linked pedigrees and Davison (1973) suggested that the cause of nonspecific mental retardation (MR) may be due to an X-linked etiology, it was Lehr
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https://doi.org/10.1057/9780230272354eading to changes in plasma lipoproteins or lipoprotein receptors can result in changes in the concentration of certain lipids in the blood and tissues. The defects involved in a number of lysosomal storage diseases were discovered in the 1960s, and these initial studies have led to reliable methods
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Pam Musil,Doug Risner,Karen Schuppse disorders affect the nervous system, and mental retardation is a major finding. Others are associated with acute metabolic crisis. Simple diagnostic tests and effective treatment are available for many of these disorders and early intervention may prevent some of the clinical symptoms. The opport
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