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dc.contributor.authorWatson, P.en_US
dc.contributor.authorNarod, S. A.en_US
dc.contributor.authorFodde, R.en_US
dc.contributor.authorWagner, A.en_US
dc.contributor.authorLynch, J. F.en_US
dc.contributor.authorTinley, S. T.en_US
dc.contributor.authorSnyder, C. L.en_US
dc.contributor.authorCoronel, S. A.en_US
dc.contributor.authorRiley, B.en_US
dc.contributor.authorKinarsky, Y.en_US
dc.contributor.authorLynch, H. T.en_US
dc.date.accessioned2015-09-08T16:15:54Z
dc.date.available2015-09-08T16:15:54Z
dc.date.issued2003en_US
dc.identifier.citationWatson, P.; Narod, SA; Fodde, R.; Wagner, A.; Lynch, JF; Tinley, ST; Snyder, CL; Coronel, SA; Riley, B.; Kinarsky, Y.; Lynch, HT. Carrier risk status changes resulting from mutation testing in hereditary non-polyposis colorectal cancer and hereditary breast-ovarian cancer. Journal of medical genetics. 2003, AUG. 40(8):591-596.en_US
dc.identifier.issn0022-2593en_US
dc.identifier.issn1468-6244en_US
dc.identifier.urihttp://hdl.handle.net/10504/71580
dc.titleCarrier risk status changes resulting from mutation testing in hereditary non-polyposis colorectal cancer and hereditary breast-ovarian canceren_US
dc.typeJournal Articleen_US
dc.description.volume40en_US
dc.title.workJournal of Medical Geneticsen_US
dc.description.pages591-596en_US
dc.date.year2003en_US
dc.date.monthAugusten_US
dc.description.issue8en_US
dc.program.unitSchool of Medicineen_US
dc.program.unitPreventive Medicineen_US
dc.url.link1http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1735553en_US
dc.contributor.cuauthorLynch, Henry T.en_US
dc.contributor.cuauthorRiley, Bronsonen_US
dc.contributor.cuauthorWatson, Patriceen_US
dc.contributor.cuauthorTinley, Susan T.en_US
dc.contributor.cuauthorSnyder, Carrie L.en_US
dc.contributor.cuauthorCoronel, Stephanie M.en_US
dc.contributor.cuauthorKinarsky, Yuliaen_US
dc.contributor.cuauthorLynch, Jane F.en_US
dc.identifier.pmid12920070en_US


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