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dc.creatorBottis, Maria Canellopoulouen
dc.date.accessioned2011-07-12T18:22:30Zen
dc.date.available2011-07-12T18:22:30Zen
dc.date.created2000-06en
dc.date.issued2000-06en
dc.identifier.bibliographicCitationEuropean Journal of Health Law 2000 June; 7(2): 173-183en
dc.identifier.urihttp://hdl.handle.net/10822/514760en
dc.formatArticleen
dc.languageengen
dc.source218881en
dc.subjectAutonomyen
dc.subjectBeneficenceen
dc.subjectConfidentialityen
dc.subjectGenetic Informationen
dc.subjectRight Not To Knowen
dc.subject.classificationPhilosophical Ethicsen
dc.subject.classificationTruth-tellingen
dc.subject.classificationConfidentialityen
dc.subject.classificationGenetic Screening / Genetic Testingen
dc.titleComment on a View Favoring Ignorance of Genetic Information: Confidentiality, Autonomy, Beneficence and the Right Not to Knowen
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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