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dc.contributor.authorSchehl, Colleen Marie
dc.date.accessioned2014-09-29T19:41:16Z
dc.date.available2014-09-29T19:41:16Z
dc.date.issued1997-07-01
dc.identifier.urihttps://hdl.handle.net/11244/12374
dc.description.abstractThe objective ofthis study was to determine the incidence of unique gennline mutations in the BRCAI and retinoblastoma (Rb) tumor suppressor genes in Japanese women diagnosed with ovarian cancer by Single-Strand Confonnation Polymorphism (SSCP) analysis. This thesis has been prepared as two chapters that have been submitted as two manuscripts. The first manuscript was submitted with collaborators to Human Mutation and the second manuscript was submitted to Cancer.
dc.formatapplication/pdf
dc.languageen_US
dc.publisherOklahoma State University
dc.rightsCopyright is held by the author who has granted the Oklahoma State University Library the non-exclusive right to share this material in its institutional repository. Contact Digital Library Services at lib-dls@okstate.edu or 405-744-9161 for the permission policy on the use, reproduction or distribution of this material.
dc.titlePotential Involvement of the Breast Cancer (BRCAl) and Retinoblastoma (Rb) Tumor Suppressor Genes in the Hereditary Predisposition to Ovarian Cancer in Japanese Women
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osu.filenameThesis-1997-S317p.pdf
osu.accesstypeOpen Access
dc.type.genreThesis


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