Genetic information : acquisition, access, and control /

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Bibliographic Details
Imprint:New York : Kluwer Academic/Plenum Publishers, c1999.
Description:xi, 335 p. ; 26 cm.
Language:English
Subject:
Format: Print Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/4259039
Hidden Bibliographic Details
Other authors / contributors:Thompson, Alison K.
Chadwick, Ruth F.
ISBN:0306460521
Notes:Includes bibliographical references and index.
Table of Contents:
  • Eugenics
  • 1. Can we Learn from Eugenics?
  • 2. Preventing Genetic Impairments: Does it Discriminate against People with Disabilities?
  • Genetics and Insurance
  • 3. Private Parties, Public Duties? The Shifting Role of Insurance Companies in the Genetics Era
  • 4. Coercion Control, and Consequence in Genetic Testing: Views on Insurance among Tested Individuals and the General Public
  • 5. Genetic Testing and Adverse Selection in the Market for Life Insurance: Preliminary Findings for the BRCA1 Gene Mutation
  • 6. Genetic Engineering and German Health Insurances
  • 7. Selling Souls: Ethical Theory and the Commercialisation of Genetic Information
  • The Commercialization of Genetic Information
  • 8. The Ethics of 21st Century Bioinformatics: Ethical Implications of the Vanishing Distinction between Biological Information and Other Information
  • 9. There is Nothing Special about Genetic Information
  • 10. High Speed Genetic Testing Technology and the Computerization of the Medical Record
  • 11. Ethical Questions in the Pursuit of Genetic Information: Geneticization and BRCA1
  • 12. The Ethics of Gene Patenting
  • 13. Paradigms of Author/Creator Property Rights in Intellectual Property Law: Ethical Implications for the Acquisition, Access, and Control of Genetic Information
  • 14. Regulating the Commercialization of Human Genetics: Can We Address the Big Concerns?
  • 15. Ethical Impacts of Human Health-Related Biotechnology in Brazil
  • Public Awareness
  • 16. Adolescents and Carrier Testing: Attitudes and Ethical Presuppositions
  • 17. Downs Syndrome Screening: How Do They Know?
  • 18. Public Perspectives of the New Genetics: The Citizens Jury Experiment
  • 19. Genetics and Journalism: A View from the United States
  • Theoretical Concerns
  • 20. Genetic Information and `Genetic Identity'
  • 21. Genetic Information and Knowing when you will Die
  • 22. Influences of Genetic Testing on a Persons Freedom
  • 23. Genetic Knowledge: The Contribution of Sociologies
  • 24. Germ-Line gene Therapy: Is the Existing UK Norm Ethically Valid?
  • 25. Negotiating the Dilemmas of Prenatal Testing for Genetic Disorders: What is the Virtuous Person to Do?
  • 26. Genetic Information: Questions and Worries from an African Background
  • 27. Genetic Knowledge in a Just Society
  • 28. Biotechnology, Genetic Information, and Community: From Individual Rights to Social Duties
  • 29. Linear Destiny and Geometric Fate
  • 30. A New Framework for the Use of Genetic Information
  • Index