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dc.creatorSchillinger, Deanen
dc.creatorDohan, Danielen
dc.date.accessioned2011-07-12T18:21:37Zen
dc.date.available2011-07-12T18:21:37Zen
dc.date.created2008-06en
dc.date.issued2008-06en
dc.identifierhttp://bioethics.neten
dc.identifier.bibliographicCitationAmerican Journal of Bioethics 2008 June; 8(6): 12-14en
dc.identifier.urihttp://hdl.handle.net/10822/512995en
dc.formatArticleen
dc.languageengen
dc.source316781en
dc.subjectGenetic Testingen
dc.subjectVulnerable Populationsen
dc.subject.classificationGenetic Screening / Genetic Testingen
dc.subject.classificationBusiness Ethicsen
dc.subject.classificationHealth Care Programs for Womenen
dc.titleGenetic testing for vulnerable populations: what kinds of communications we need and do not needen
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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