Show simple item record

dc.creatorKent, Alastairen
dc.date.accessioned2011-07-12T18:36:14Zen
dc.date.available2011-07-12T18:36:14Zen
dc.date.created1999en
dc.date.issued1999en
dc.identifier.bibliographicCitationIn: Nippert, I.; Neitzel, H.; Wolff, G., eds. The New Genetics: From Research into Health Care: Social and Ethical Implications for Users and Providers. New York: Springer; 1999: 119-123.en
dc.identifier.urihttp://hdl.handle.net/10822/534524en
dc.formatBook Chapteren
dc.languageengen
dc.source197150en
dc.subjectGenetic Testingen
dc.subjectPatientsen
dc.subject.classificationGenetic Screening / Genetic Testingen
dc.titleThe patients' perspective on the provision of genetic testing.en
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


This item appears in the following Collection(s)

Show simple item record


Georgetown University Seal
©2009—2019 Bioethics Research Library
Box 571212 Washington DC 20057-1212
202.687.3885