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dc.contributor.authorLacroix, Mireille
dc.contributor.authorGodard, Béatrice
dc.contributor.authorKnoppers, Bartha Maria
dc.date.accessioned2008-04-15T19:54:10Z
dc.date.available2008-04-15T19:54:10Z
dc.date.issued2005
dc.identifier.citationLACROIX Mireille, Béatrice GODARD et Bartha Maria KNOPPERS, "Warning Patients’ Relatives of Genetic Risks: Policy Approaches", (2005), GenEdit, III-3, I-8en
dc.identifier.urihttp://hdl.handle.net/1866/2267
dc.format.extent237529 bytes
dc.format.mimetypeapplication/pdf
dc.publisherGenEditen
dc.subjectFamily
dc.subjectGenetic testing
dc.subjectRisk
dc.subjectCommunication
dc.subjectInformation
dc.titleWarning Patients’ Relatives of Genetic Risks: Policy Approachesen
dc.typeArticleen
dc.contributor.affiliationUniversité de Montréal. Faculté de droit. Centre de recherche en droit publicfr
dc.contributor.affiliationUniversité de Montréal. Faculté de droitfr
dcterms.abstractAs an increasing number of genetic tests for specific early- and late-onset disorders move from research to the clinical setting, health care professionals are faced with new challenges or, alternatively, with novel twists on age-old ethical dilemmas. A finding that an individual carries a deleterious mutation can indicate that his or her relatives are at an increased risk of being affected by the same genetic disorder.en
dcterms.description[À l'origine dans / Was originally part of : CRDP - Droit, biotechnologie et rapport au milieu]fr
dcterms.languageengen
UdeM.VersionRioxxVersion acceptée / Accepted Manuscript


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