Genetics, Society And Clinical

Genetics, Society And Clinical

Buch | Softcover
264 Seiten
1997
Bios Scientific Publishers Ltd (Verlag)
978-1-85996-206-0 (ISBN)
32,40 inkl. MwSt
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This volume examines, from both ethical and clinical perspectives, the impact of increasing genetic knowledge on individuals and families. The authors describe the social implications arising from the ability to test for an increasing number of genetic diseases.
This volume examines, from both ethical and clinical perspectives, the impact of increasing genetic knowledge on individuals and families. The authors use their experience of working within clinical genetics to describe the social implications arising from the ability to test for an increasing number of genetic diseases. Current controversial issues are described. Several chapters are based on lead articles and editorials the authors have been asked to write for "The Lancet" and the "British Medical Journal". The book provides an introduction to the effects on individuals of the practical issues associated with genetic testing and should, therefore, be of interest to all those involved in clinical genetics.

What do we mean by genetic testing?; pre-symptomatic testing for late onset disorder - lessons from Huntingdon's disease; genetic testing and insurance; population screening for carriers and for genetic susceptibility to disease; issues in newborn screening; genetic counselling - is it possible to be non-directive?; genetics of IQ; naming of genetic syndromes - the case of Hallervorden-Spatz; Huntingdon's disease and the abuse of genetics; China's new genetics law. (Part contents)

Erscheint lt. Verlag 15.6.1997
Zusatzinfo 2ill.
Verlagsort London
Sprache englisch
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Medizinethik
Studium 2. Studienabschnitt (Klinik) Humangenetik
Studium Querschnittsbereiche Geschichte / Ethik der Medizin
ISBN-10 1-85996-206-8 / 1859962068
ISBN-13 978-1-85996-206-0 / 9781859962060
Zustand Neuware
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