Buch, Englisch, 336 Seiten, Paperback, Format (B × H): 155 mm x 235 mm, Gewicht: 534 g
Acquisition, Access, and Control
Buch, Englisch, 336 Seiten, Paperback, Format (B × H): 155 mm x 235 mm, Gewicht: 534 g
ISBN: 978-1-4757-7178-7
Verlag: Springer US
Zielgruppe
Research
Autoren/Hrsg.
Fachgebiete
- Rechtswissenschaften Öffentliches Recht Medizin- und Gesundheitsrecht
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Medizin, Gesundheitswesen Medizinrecht, Gesundheitsrecht
- Geisteswissenschaften Philosophie Ethik, Moralphilosophie
- Naturwissenschaften Biowissenschaften Biowissenschaften Bioethik, Tierethik
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Medizin, Gesundheitswesen Public Health, Gesundheitsmanagement, Gesundheitsökonomie, Gesundheitspolitik
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Vorklinische Medizin: Grundlagenfächer Humangenetik
Weitere Infos & Material
Eugenics. 1. Can we Learn from Eugenics? D. Wikler. 2. Preventing Genetic Impairments: Does it Discriminate against People with Disabilities? H. Kuhse. Genetics and Insurance. 3. Private Parties, Public Duties? The Shifting Role of Insurance Companies in the Genetics Era; T. Lemmens. 4. Coercion Control, and Consequence in Genetic Testing: Views on Insurance among Tested Individuals and the General Public; R.N. Mayer, et al. 5. Genetic Testing and Adverse Selection in the Market for Life Insurance: Preliminary Findings for the BRCA1 Gene Mutation; K.R. Smith, et al. 6. Genetic Engineering and German Health Insurances; T. Uhlemann. 7. Selling Souls: Ethical Theory and the Commercialisation of Genetic Information; M. Johnston. The Commercialization of Genetic Information. 8. The Ethics of 21st Century Bioinformatics: Ethical Implications of the Vanishing Distinction between Biological Information and Other Information; D. Holdsworth. 9. There is Nothing Special about Genetic Information; S. Holm. 10. High Speed Genetic Testing Technology and the Computerization of the Medical Record; C.R. Naser. 11. Ethical Questions in the Pursuit of Genetic Information: Geneticization and BRCA1; S. Sherwin, C. Simpson. 12. The Ethics of Gene Patenting; R. Macklin. 13. Paradigms of Author/Creator Property Rights in Intellectual Property Law: Ethical Implications for the Acquisition, Access, and Control of Genetic Information; R. Mackenzie. 14. Regulating the Commercialization of Human Genetics: Can We Address the Big Concerns? T. Caulfield. 15. Ethical Impacts of Human Health-Related Biotechnology in Brazil; M. Bernardes Marques. Public Awareness. 16. Adolescents and Carrier Testing: Attitudes and Ethical Presuppositions; K. Dierickx. 17. Downs Syndrome Screening: How Do They Know? R. Bramwell, S. Wade. 18. Public Perspectives of the New Genetics: The Citizens Jury Experiment; R. Iredale, M. Longley. 19. Genetics and Journalism: A View from the United States; J. Stephenson. Theoretical Concerns. 20. Genetic Information and `Genetic Identity'; R.E. Ashcroft. 21. Genetic Information and Knowing when you will Die; M.P. Battin. 22. Influences of Genetic Testing on a Persons Freedom; E. Hilt. 23. Genetic Knowledge: The Contribution of Sociologies; S. Dyson. 24. Germ-Line gene Therapy: Is the Existing UK Norm Ethically Valid? S. Dziobon. 25. Negotiating the Dilemmas of Prenatal Testing for Genetic Disorders: What is the Virtuous Person to Do? A. Gallagher. 26. Genetic Information: Questions and Worries from an African Background; G.B. Tangwa. 27. Genetic Knowledge in a Just Society; N. Holtug. 28. Biotechnology, Genetic Information, and Community: From Individual Rights to Social Duties; S.K. Hellsten. 29. Linear Destiny and Geometric Fate; E. Mordini. 30. A New Framework for the Use of Genetic Information; J.A.K. Kegley. Index.