Preventing genetically transmitted disabilities while respecting persons with disabilities

Quality of Life and Human Difference: Genetic Testing, Health Care, and Disability

Volumn , Issue , 2005, Pages 67-100

  Brock, Dan W ^a  

^a HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84926986836     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1017/CBO9780511614590.004     Document Type: Chapter

References (19)

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2. Brock, D.W. 1988. “Ethical Issues in Recipient Selection for Organ Transplantation.” In D. Mathieu (ed.), Organ Substitution Technology: Ethical, Legal and Public Policy Issues. Boulder, CO and London:Westview Press, pp. 86-99.
3. Brock, D.W. 1993. “Quality of Life Measures in Health Care and Medical Ethics.” In A. Sen and M. Nussbaum (eds.), The Quality of Life. Oxford: Oxford University Press, pp. 95-132.
4. Brock, D. W. 1994. “Reproductive Freedom: Its Nature, Bases, and Limits.” In David Thomasma and John Monagle (eds.), Healthcare Ethics: Critical Issues for Health Professionals. Gaithersburg, MD: Aspen Publishers, pp. 43-61.
5. Brock, D. W. 1995. “The Non-Identity Problem and Genetic Harm.” Bioethics9: 269-75.
6. Brock, D. W. 2000. “Health Care Resource Prioritization and Discrimination against Persons with Disabilities.” In L. Francis and A. Silvers (eds.), Americans with Disabilities: Implications for Individuals and Institutions. New York: Routledge, pp. 223-35.
7. Brock, D. W. 2004. “Ethical Issues in the Use of Cost Effectiveness Analysis for the Prioritization of Health Care Resources.” In T. Tan-Torres et al. (eds.), Making Choices in Health: WHO Guide to Cost-Effectiveness Analysis. Geneva: World Health Organisation.
8. Buchanan, A. E., Brock, D. W., Daniels, N., and Wikler, D. 2000. From Chance to Choice: Genes and Social Justice. Cambridge: Cambridge University Press.
9. Griffin, J. 1986. Well-Being. Oxford: Clarendon Press.
10. McMahan, J. 1998. “Wrongful Life: Paradoxes in the Morality of Causing People to Exist.” In J. Coleman and C. Morris (eds.), Rational Commitment and Social Justice: Essays for Gregory Kavka. Cambridge: Cambridge University Press.
11. McMahan, J. 2002. The Ethics of Killing. Oxford: Oxford University Press.
12. Murray, C. J. L. 1996. “Rethinking DALYs.” In C. J. L. Murray and A. D. Lopez (eds.), The Global Burden of Disease. Cambridge, MA and Geneva: Harvard School of Public Health and World Health Organization.
13. National Organization on Disability. 1994. National Organization on Disability/Louis Harris Survey of Americans with Disabilities. New York: Louis Harris and Associates.
14. Parfit, D. 1984. Reasons and Persons, Oxford: Clarendon Press.
15. Peters, P. G. 1989. “Protecting the Unconceived: Nonexistence, Avoidability, and Reproductive Technology.” Arizona Law Review31 (3): 487-548.
16. Roe V. Wade, 410 U. S. 113 (1973).
17. Sackett, D. L., and Torrance, G. W. 1978. “The Utility of Different Health States as Perceived by the General Public.” Journal of Chronic Diseases31: 697-704.
18. Silvers, A. 1994. “Defective Agents: Equality, Difference and the Tyranny of the Normal.” Journal of Social Philosophy (twenty-fifth anniversary special issue): 154-75.
19. Silvers, A. 1998. “Formal Justice.” In A. Silvers, D. Wasserman, and M. Mahowald (eds.), Disability, Difference, Discrimination. Lanham, MD: Rowman and Littlefield, pp. 13-145.