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dc.creatorBreithaupt, Holgeren
dc.date.accessioned2011-07-12T18:24:14Zen
dc.date.available2011-07-12T18:24:14Zen
dc.date.created2001-06en
dc.date.issued2001-06en
dc.identifierhttp://embo-reports.oupjournals.org/cgi/content/full/2/6/46 5en
dc.identifier.bibliographicCitationEMBO Reports 2001 June; 2(6): 465-467en
dc.identifier.urihttp://hdl.handle.net/10822/518494en
dc.formatArticleen
dc.languageengen
dc.source232622en
dc.subjectDatabasesen
dc.subjectGenetic Databasesen
dc.subjectHealthen
dc.subjectHealth Careen
dc.subjectMedicineen
dc.subjectQuality Of Health Careen
dc.subject.classificationConfidentialityen
dc.subject.classificationQuality of Health Careen
dc.subject.classificationGenetics, Molecular Biology and Microbiologyen
dc.subject.classificationBehavioral Geneticsen
dc.subject.classificationInformation Science Ethicsen
dc.subject.classificationEconomics of Health Careen
dc.titleThe future of medicine. Centralised health and genetic databases promise to increase quality of health care while lowering costs. But to get there, many legal and social obstacles will have to be overcome to prevent abuseen
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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