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dc.creatorJepson, Ruth G.en
dc.creatorForbes, Carol A.en
dc.creatorSowden, Amanda J.en
dc.creatorLewis, Ruth A.en
dc.date.accessioned2011-07-12T18:24:18Zen
dc.date.available2011-07-12T18:24:18Zen
dc.date.created2001-06en
dc.date.issued2001-06en
dc.identifier.bibliographicCitationHealth Expectations 2001 June; 4(2): 116-126en
dc.identifier.urihttp://hdl.handle.net/10822/518668en
dc.formatArticleen
dc.languageengen
dc.source233397en
dc.subjectReviewen
dc.subject.classificationTechnology Assessmenten
dc.subject.classificationSociology of Health Careen
dc.subject.classificationGenetic Counseling / Prenatal Diagnosisen
dc.subject.classificationGenetic Screening / Genetic Testingen
dc.subject.classificationResearch on Special Populationsen
dc.subject.classificationInformed Consenten
dc.subject.classificationHealth Care for Particular Diseases or Groupsen
dc.titleIncreasing informed uptake and non-uptake of screening: evidence from a systematic reviewen
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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