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  1. A. A. Scitovsky, A. M. Capron & Anne A. Scitovsky (forthcoming). An Ethical Perspective. Scarce Medical Resources and Justice.
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  2. A. M. Capron (2008). Legal and Regulatory Standards of Informed Consent in Research. In Ezekiel J. Emanuel (ed.), The Oxford Textbook of Clinical Research Ethics. Oxford University Press. 613--32.
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  3. A. M. Capron (2004). When Experiments Go Wrong: The US Perspective. Journal of Clinical Ethics 15 (1):22.
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  4. A. M. Capron (2000). Genetics and Insurance: Accessing and Using Private Information. Social Philosophy and Policy 17 (02):235-.
    Is information about a person's genome, whether derived from the analysis of DNA or otherwise, protected by the right to privacy? If it is, why and in what manner? It often appears that some people believe that the answer to this question is to be found in molecular genetics itself. They point to the rapid progress being made in basic and applied aspects of this field of biology; this progress has remarkably increased what is known about human genetics. Since knowledge (...)
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  5. A. M. Capron (1996). A Matter of Law? Reply. Hastings Center Report 26 (3):2-2.
     
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  6. A. M. Capron (1996). After the Fact-Reply. Hastings Center Report 26 (3):3-3.
     
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  7. A. M. Capron (1991). Protection of Research Subjects: Do Special Rules Apply in Epidemiology? Journal of Law, Medicine and Ethics 19 (3-4):184-190.
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  8. A. M. Capron (1990). Criteria of Death. Journal of Medical Ethics 16 (3):167-167.
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  9. A. M. Capron (1990). Reflections on Health Law and Ethics. Journal of Law, Medicine and Ethics 18 (1-2):15-19.
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  10. A. M. Capron (1990). The New Ethical Lnstitutions. Lnternational Journal of Bioethics 50:43.
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  11. A. M. Capron & M. J. Radin (1988). Choosing Family Law Over Contract Law as a Paradigm for Surrogate Motherhood. Journal of Law, Medicine and Ethics 16 (1-2):34-43.