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dc.creatorErsig, Anne Len
dc.creatorAyres, Lionessen
dc.creatorHadley, Donald Wen
dc.creatorKoehly, Laura Men
dc.date.accessioned2011-07-12T18:22:55Zen
dc.date.available2011-07-12T18:22:55Zen
dc.date.created2010-06en
dc.date.issued2010-06en
dc.identifier1547-5069en
dc.identifier10.1111/j.1547-5069.2010.01342.xen
dc.identifier.bibliographicCitationJournal of nursing scholarship : an official publication of Sigma Theta Tau International Honor Society of Nursing / Sigma Theta Tau 2010 Jun; 42(2): 139-46en
dc.identifier.urihttp://hdl.handle.net/10822/515691en
dc.description.abstractGenetic testing for hereditary forms of cancer does not always identify a causative mutation. Little is known about personal or family response to these indeterminate results when a hereditary form of cancer is suspected. This study explored thoughts about and responses to risk for hereditary nonpolyposis colorectal cancer (HNPCC) when a family member has received indeterminate genetic test results.en
dc.description.urihttp://dx.doi.org/10.1111/j.1547-5069.2010.01342.xen
dc.formatArticleen
dc.languageengen
dc.source332863en
dc.subjectCanceren
dc.subjectFormsen
dc.subjectGenetic Testingen
dc.subjectMutationen
dc.subjectRisken
dc.subject.classificationConcept of Healthen
dc.subject.classificationGenetic Screening / Genetic Testingen
dc.subject.classificationNeurosciences and Mental Health Therapiesen
dc.titleExplanations of risk in families without identified mutations for hereditary nonpolyposis colorectal cancer.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


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