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dc.contributor.authorSaukko, P. M.en
dc.contributor.authorEllard, Sianen
dc.contributor.authorRichards, S. H.en
dc.contributor.authorShepherd, Maggieen
dc.contributor.authorCampbell, John L.en
dc.date.accessioned2016-09-02T10:10:38Z
dc.date.available2016-09-02T10:10:38Z
dc.date.issued2007
dc.identifier.citationPatients' understanding of genetic susceptibility testing in mainstream medicine: qualitative study on thrombophilia. 2007, 7:82 BMC Health Serv Resen
dc.identifier.issn1472-6963
dc.identifier.pmid17565670
dc.identifier.doi10.1186/1472-6963-7-82
dc.identifier.urihttp://hdl.handle.net/11287/619270
dc.description.abstractUK and US policy initiatives have suggested that, in the future, patients and clinicians in mainstream medicine could use genetic information to prevent common illnesses. There are no studies on patients' experience and understanding of the process of testing for common genetic susceptibilities in mainstream medicine.en
dc.language.isoenen
dc.publisherBioMed Centralen
dc.relation.urlhttp://bmchealthservres.biomedcentral.com/articles/10.1186/1472-6963-7-82en
dc.rightsArchived with thanks to BMC health services researchen
dc.subjectWessex Classification Subject Headings::Oncology. Pathology.::Geneticsen
dc.titlePatients' understanding of genetic susceptibility testing in mainstream medicine: qualitative study on thrombophilia.en
dc.typeResearch Support, Non-U.S. Gov'ten
dc.identifier.journalBMC health services researchen
dc.description.noteThis article is freely available via Open Access. Click on the ‘Additional Link’ above to access the full-text from the publisher’s site.en
dc.description.fundingPDA/02/06/098/Department of Health/United Kingdomen
dc.type.versionPublisheden


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