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dc.creatorHelmes, Almut W.en
dc.creatorBowen, Deborah J.en
dc.creatorBengel, Jurgenen
dc.date.accessioned2011-07-12T18:25:20Zen
dc.date.available2011-07-12T18:25:20Zen
dc.date.created2002-05en
dc.date.issued2002-05en
dc.identifier.bibliographicCitationGenetics in Medicine 2002 May-June; 4(3): 150-157en
dc.identifier.urihttp://hdl.handle.net/10822/520868en
dc.formatArticleen
dc.languageengen
dc.source245970en
dc.subjectBreast Canceren
dc.subjectCanceren
dc.subjectGenetic Testingen
dc.subjectRisken
dc.subject.classificationPhilosophical Ethicsen
dc.subject.classificationPatient Relationshipsen
dc.subject.classificationGenetic Screening / Genetic Testingen
dc.subject.classificationInformed Consenten
dc.subject.classificationHealth Care Programs for Womenen
dc.titlePatient preferences of decision-making in the context of genetic testing for breast cancer risken
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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