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dc.creatorZeps, Nikolajsen
dc.creatorIacopetta, Barry J.en
dc.creatorSchofield, Lynen
dc.creatorGeorge, Jillian M.en
dc.creatorGoldblatt, Jacken
dc.date.accessioned2011-07-12T18:20:25Zen
dc.date.available2011-07-12T18:20:25Zen
dc.date.created2007-01-15en
dc.date.issued2007-01-15en
dc.identifier0025-729Xen
dc.identifier.bibliographicCitationMedical Journal of Australia 2007 January 15; 186(2): 88-90en
dc.identifier.urihttp://hdl.handle.net/10822/510542en
dc.formatArticleen
dc.languageengen
dc.source304289en
dc.subjectConsenten
dc.subjectResearchen
dc.subjectRightsen
dc.subject.classificationGenetics, Molecular Biology and Microbiologyen
dc.subject.classificationGenetic Screening / Genetic Testingen
dc.subject.classificationInformed Consent or Human Experimentationen
dc.titleWaiver of individual patient consent in research: when do potential benefits to the community outweigh private rights?en
dc.provenanceDigital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National Human Genome Research Instituteen
dc.provenanceDigital citation migrated from OpenText Livelink Discovery Server database named GenETHX to DSpace collection GenETHX hosted by Georgetown Universityen


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