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Information that Should be Given to HIV Cohort Participants During Ongoing Research: The Viewpoints of Patient Representatives and Research Professionals.Journal of Empirical Research on Human Research Ethics, 2011, 6 (4), pp.76-83. ⟨10.1525/jer.2011.6.4.76⟩
Journal articles
inserm-00658527v1
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Ethical issues related to computerised family medical histories in sickle cell disease: Inforare.Journal of Medical Ethics, 2010, 36 (10), pp.604-7. ⟨10.1136/jme.2009.034066⟩
Journal articles
istex
inserm-00612293v1
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