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Titlebook: Genetic Disorders, Syndromology and Prenatal Diagnosis; T. V. N. Persaud Book 1982 MTP Press Limited 1982 development.embryo.embryology.ep

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發(fā)表于 2025-3-21 17:28:58 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Genetic Disorders, Syndromology and Prenatal Diagnosis
編輯T. V. N. Persaud
視頻videohttp://file.papertrans.cn/383/382482/382482.mp4
叢書名稱Advances in the Study of Birth Defects
圖書封面Titlebook: Genetic Disorders, Syndromology and Prenatal Diagnosis;  T. V. N. Persaud Book 1982 MTP Press Limited 1982 development.embryo.embryology.ep
描述Birth defects have assumed an importance even greater now than in the past because infant mortality rates attributed to congenital anomalies have declined far less than those for other causes of death, such as infectious and nutritional diseases. As many as 50 % of all pregnancies terminate as miscarriages, and in the majority of cases this is the result of faulty intrauterine development. Major congenital malformations are present in at least 2 % of all liveborn infants, and 22 % of all stillbirths and infant deaths are associated with severe congenital anomalies. Not surprisingly, there has been a great proliferation of research into the problems of developmental abnormalities over the past few decades. This series, Advances in the Study of Birth Defects, was conceived in order to provide a comprehensive focal source of up-to-date information for physi- cians concerned with the health of the unborn child and for research workers in the fields of fetal medicine and birth defects. The first four volumes featured recent experimental work on selected areas of high priority and intensive investigation, including mechanisms of teratogenesis, teratological evaluation, molecular and cell
出版日期Book 1982
關(guān)鍵詞development; embryo; embryology; epidemiology; nutrition; taxonomy
版次1
doihttps://doi.org/10.1007/978-94-011-6669-0
isbn_softcover978-94-011-6671-3
isbn_ebook978-94-011-6669-0
copyrightMTP Press Limited 1982
The information of publication is updating

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發(fā)表于 2025-3-21 20:33:22 | 只看該作者
Zugeordnete Normalprojektionen,The cytogenetics of several recessive inheritance disease states in human will be discussed. These diseases belong to the categories of (1) autosomal recessive and (2) X-linked recessive disorders.
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Helmut Winterhager,Hans-Peter KrugThe process of syndrome delineation can be divided into the following stages:
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Chromosomal abnormalities in single gene disorders,The cytogenetics of several recessive inheritance disease states in human will be discussed. These diseases belong to the categories of (1) autosomal recessive and (2) X-linked recessive disorders.
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Prenatal diagnosis of genetic diseases by amniocentesis,Prenatal diagnosis is now possible for a considerable number of genetic diseases and/or birth defects using a variety of techniques.
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發(fā)表于 2025-3-23 00:03:21 | 只看該作者
https://doi.org/10.1007/978-3-662-30331-3chromatic regions, especially the short arm and satellite regions of the acrocentric chromosomes and the long arm of the Y chromosome. The advent of new staining techniques has helped in the identification of sites of morphological variation in human chromosomes. The variable segments correspond to
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Maria Lipp,Karl-Heinz Maria Tillwichabnormal development of the aborted conceptus in these cases has been well documented since the time of Mall in 1908. who also observed that the frequency of anomalies is directly proportional to the developmental age of the conceptus. In the aborted embryo the incidence is over 80%, declining throu
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