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  • Identifying People's Genes:Ethical Aspects of DNA Sampling in Populations
  • Patricia A. Baird, Professor
Patricia A. Baird, Professor
Department of Medical Genetics, Faculty of Medicine, University of British Columbia, #222-6174 University Boulevard, Vancouver, B.C. V6T 1Z3, Canada

References

1. HOLTZMAN, N. A. Proceed with Caution. Baltimore: Johns Hopkins Univ. Press, 1989.
2. BEAUCHAMP, T. L., and CHILDRESS, J. F. Principles of Biomedical Ethics. 3d ed. New York: Oxford Univ. Press, 1989.
3. FRANCOEUR, R. Biomedical Ethics: A guide to Decision-Making. New York: John Wiley, 1983.
4. MAPPES, T. A., and ZEMBATY, J. S. Biomedical Ethics. 3d ed. New York: McGraw-Hill, 1991.
5. EVANS, R. G., and STODDART, G. L. Producing health, consuming health care. Soc. Sci. and Med. 31 (12): 1347-1363, 1990.
6. KNOX, E. G. The confidentiality of medical records: The principles and practice of protection in a research dependent environment. Report of the Working Party of Advisory Panel for Social Medicine and Epidemiology in European Economic Community. Luxemburg: Commission of the European Communities 1984.
7. Proceed with Care: Final Report of the Royal Commission on New Reproductive Technologies. Ch. 3. 1993.
8. Declaration of Helsinki. Recommendations Guiding Doctors in Biomedical Research Involving Human Subject. Adopted by the 18th World Medical Assembly, Helsinki, Finland, 1964, and as revised by the 29th World Medical Assembly, Tokyo, Japan, 1975.
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10. John Moore vs. Regents of University of California et al, July 9, 1990, SCC (File S006987), 202 Cal App 3d 1230; 249 Cal Rptr 494 (1988).
11. The Queen vs. Dyment (1988) 2 SCR 417.
12. KNOPPERS, B. M., and LABERGE, C. DNA sampling and informed consent. CMAJ 140:1023-1028, 1989.
13. FLETCHER, J. C., and WERTZ, D. C. Ethics, law and medical genetics: After the human genome is mapped. Emory Law J. 39:747-809, 1990.
14. Presidents' Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioural Research. Screening and counselling for genetic conditions: The ethical, social and legal implications of genetic screening, counselling, and education programs. Washington, D.C.: U.S. Government Printing Office, 1983.
15. MCEWEN, J. E., and REILLY, P. R. State legislature efforts to regulate use and potential misuse of genetic information. AJ Hum. Genet. 51:637-647, 1992.
16. HOUSE, J., et al. Social relationships and health. Science 241:540-545, 1988.
17. MARMOT, M. G., and THEORELL, T. Social class and cardiovascular disease: The contribution of work. Internat. J. Health Sci. 18(4):659-674, 1988.
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Additional Information

ISSN
1529-8795
Print ISSN
0031-5982
Pages
pp. 159-166
Launched on MUSE
2015-01-07
Open Access
No
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