Genetics, Society And Clinical
Seiten
1997
Bios Scientific Publishers Ltd (Verlag)
978-1-85996-206-0 (ISBN)
Bios Scientific Publishers Ltd (Verlag)
978-1-85996-206-0 (ISBN)
- Titel ist leider vergriffen;
keine Neuauflage - Artikel merken
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.
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 |
Haben Sie eine Frage zum Produkt? |
Mehr entdecken
aus dem Bereich
aus dem Bereich
Eine sehr persönliche Geschichte | Der New York Times-Bestseller
Buch | Softcover (2023)
Ullstein Taschenbuch Verlag
21,99 €
Die revolutionäre Medizin von morgen (Lifespan)
Buch | Softcover (2020)
DuMont Buchverlag
16,00 €