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Clinical utility and full disclosure of genetic results to research participants
American Journal of Bioethics 6 (6):42 – 44 (2006)
Abstract
This Article does not have an abstractDOI
10.1080/15265160600938443
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Citations of this work
Consulting communities on feedback of genetic findings in international health research: sharing sickle cell disease and carrier information in coastal Kenya. [REVIEW]Vicki Marsh, Francis Kombe, Raymond Fitzpatrick, Thomas N. Williams, Michael Parker & Sassy Molyneux - 2013 - BMC Medical Ethics 14 (1):41.
Relationships with test-tubes: Where's the reciprocity?Kelly Fryer-Edwards & Stephanie M. Fullerton - 2006 - American Journal of Bioethics 6 (6):36 – 38.
Considering the nature of individual research results.Laura M. Beskow - 2006 - American Journal of Bioethics 6 (6):38 – 40.
A review of ethical frameworks for the disclosure of individual research results in population-based genetic and genomic research. [REVIEW]Isabelle Budin-Ljøsne - 2012 - Research Ethics 8 (1):25-42.
Biobanking and Privacy Law in Brazil.Sueli Gandolfi Dallari, Felipe Angel Bocchi Castellaro & Iara Coelho Zito Guerriero - 2015 - Journal of Law, Medicine and Ethics 43 (4):714-725.
References found in this work
Disclosing individual genetic results to research participants.Vardit Ravitsky & Benjamin S. Wilfond - 2006 - American Journal of Bioethics 6 (6):8 – 17.
Informing Study Participants of Research Results: An Ethical Imperative.Conrad V. Fernandez, Eric Kodish & Charles Weijer - 2003 - IRB: Ethics & Human Research 25 (3):12.
Involving Study Populations in the Review of Genetic Research.Richard R. Sharp & Morris W. Foster - 2000 - Journal of Law, Medicine and Ethics 28 (1):41-51.
Involving Study Populations in the Review of Genetic Research.Richard R. Sharp & Morris W. Foster - 2000 - Journal of Law, Medicine and Ethics 28 (1):41-51.
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