HEC Forum 18 (1):18-36 (2006)
|Abstract||This article has no associated abstract. (fix it)|
|Keywords||Philosophy Ethics Philosophy of Medicine Theory of Medicine/Bioethics Medical Law|
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References found in this work BETA
Coding and Consent: Moral Challenges of the Database Project in Iceland.Vilhjalmur Arnason - 2004 - Bioethics 18 (1):27-49.
Institutional Review Board Assessment of Risks and Benefits Associated with Research.Ernest D. Prentice & Bruce G. Gordon - forthcoming - National Bioethics Advisory Commission 6705 Rockledge Drive, Suite 700, Bethesda, Maryland 20892-7979 Telephone: 301-402-4242• Fax: 301-480-6900• Website: Www. Bioethics. Gov.
Solidaroty and Equity : New Ethical Frameworks for Genetic Databases.Ruth Chadwick & Kåre Berg - unknown
Citations of this work BETA
Experiences with Community Engagement and Informed Consent in a Genetic Cohort Study of Severe Childhood Diseases in Kenya.V. M. Marsh, D. M. Kamuya, A. M. Mlamba, T. N. Williams & S. S. Molyneux - 2009 - BMC Medical Ethics 11 (1):13-13.
Ethical Issues in Human Genomics Research in Developing Countries.Jantina de Vries, Susan J. Bull, Ogobara Doumbo, Muntaser Ibrahim, Odile Mercereau-Puijalon, Dominic Kwiatkowski & Michael Parker - 2011 - BMC Medical Ethics 12 (1):5.
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