International Perspectives on Privacy and Access to Genetic Information

Microbial and Comparative Genomics

Volumn 2, Issue 1, 1997, Pages 53-61

  Wertz, Dorothy C ^a  

^a UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 12444301393     PISSN: 10906592     EISSN: None     Source Type: Journal    
DOI: 10.1089/omi.1.1997.2.53     Document Type: Article

References (12)

1. AMERICAN SOCIETY OF HUMAN GENETICS SOCIAL ISSUES COMMITTEE. (1997). Points to consider: Professional disclosure of familial genetic information. (Draft document, submitted.)
2. ANNAS, G. J., GLANTZ, L. H., and ROCHE, P. A. (1995). The Genetic Privacy Act and Commentary. (Boston University School of Public Health, Boston, MA).
3. BERG, K. (1989). Preface. In Ethics and Human Genetics: A Cross-Cultural Perspective. D. C. Wertz and J. C. Fletcher, eds. (Springer-Verlag, Heidelberg, Germany).
4. FLETCHER, J. C. (1989). Ethics and human genetics: A cross-cultural perspective. In Ethics and Human Genetics: A Cross-Cultural Perspective. D. C. Wertz and J. C. Fletcher, eds. (Springer-Verlag, Heidelberg, Germany).
5. ANDREWS, L. B., FULLARTON, J. E., HOLTZMAN, N. A., and MOTULSKY, A. G., eds. (1994). Assessing Genetic Risks. (National Academy of Sciences, Washington, DC).
6. LAPHAM, V., KOZMA, C., and WEISS, J. (1996). Genetic discrimination: Perspectives of consumers. Science 274, 621–624.
7. LOCKE, J. (1977). Two Treatises. Reprinted in The Locke Reader. J. W. Yolton, ed. p. 289.
8. NEW ENGLAND REGIONAL GENETICS GROUP. WERTZ, D. C., and GREGG, R., eds. (1996). Optimizing Genetics Services: Suggestions from Consumers and Providers in the New England Regional Genetics Group. (New England Regional Genetics Group, Boston, MA). The Genetic Resource 10.
9. PRESIDENT'S COMMISSION FOR THE STUDY OF ETHICAL PROBLEMS IN MEDICINE AND BIOMEDICAL AND BEHAVIORAL RESEARCH. (1983). Screening and Counseling for Genetic Conditions. (U. S. Government Printing Office, Washington, DC).
10. WERTZ, D.C. (1997). Is there a women's ethic in genetics? A 37-nation survey of providers. J Am Med Worn Assoc, 52, 33–38.
11. WERTZ, D. C., and FLETCHER, J. C., eds. (1989). Ethics and Human Genetics: A Cross-Cultural Perspective. (Springer-Verlag, Heidelberg, Germany).
12. WORLD HEALTH ORGANIZATION. WERTZ, D. C., FLETCHER, J. C., and BERG, K., eds. (1995). Guidelines on Ethical Issues in Medical Genetics and the Provision of Genetics Services. (WHO, Geneva).