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dc.creatorMcNally, Eryl; Cambon-Thomsen, Anne; Brazell, Celia; Cassiman, Jean-Jacques; Kent, Alastair; Lindpaintner, Klaus; de Faria, Paula Lobato; Niese, Detlef; Abbing, Henriette Roscam; Solbakk, Jan Helge; Tack, Helene; Tambuyzer, Erik; Weihrauch, Thomas R.; Wendel, Eriken
dc.creatorEuropean Commissionen
dc.date.accessioned2011-07-12T18:17:31Zen
dc.date.available2011-07-12T18:17:31Zen
dc.date.created2004-03en
dc.date.issued2004-03en
dc.identifier.bibliographicCitationMedical Ethics and Bioethics / Medicinska Etika & Bioetika 2004 Spring-Summer; 11(1-2): 13-18en
dc.identifier.urihttp://hdl.handle.net/10822/504475en
dc.languageeng; sloen
dc.source271038en
dc.subjectGenetic Testingen
dc.subject.classificationSocial Control of Science and Technologyen
dc.subject.classificationGenetic Screening / Genetic Testingen
dc.title25 recommendations on the ethical, legal and social implications of genetic testingen
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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