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Hereditary Cancer in Clinical Practice|December 22, 2011
Prevalence of the BRCA1 founder mutation c.5266dupin Brazilian individuals at-risk for the hereditary breast and ovarian cancer syndromeIngrid P Ewald, Patrícia Izetti, Fernando R Vargas, et al.
Hereditary Cancer in Clinical Practice|September 9, 2011
Lynch syndrome: barriers to and facilitators of screening and disease managementKathy E Watkins, Christine Y Way, Jacqueline J Fiander, et al.
Hereditary Cancer in Clinical Practice|August 9, 2011
Drug therapy for hereditary cancersEvgeny N Imyanitov, Vladimir M Moiseyenko
Hereditary Cancer in Clinical Practice|April 19, 2014
Prevalence of BRCA1 and BRCA2 mutations in unselected breast cancer patients from medellín, ColombiaJulián Esteban Londoño Hernández, Marcia Llacuachaqui, Gonzalo Vásquez Palacio, et al.
Hereditary Cancer in Clinical Practice|May 3, 2014
The Norwegian PMS2 founder mutation c.989-1G > T shows high penetrance of microsatellite instable cancers with normal immunohistochemistryEli Marie Grindedal, Harald Aarset, Inga Bjørnevoll, et al.
Hereditary Cancer in Clinical Practice|April 17, 2012
Challenges in the management of a patient with Cowden syndrome: case report and literature reviewInga Melbārde-Gorkuša, Arvīds Irmejs, Dace Bērziņa, et al.
Hereditary Cancer in Clinical Practice|August 14, 2013
Germline deletions in the EPCAM gene as a cause of Lynch syndrome - literature reviewKatarzyna Tutlewska, Jan Lubinski, Grzegorz Kurzawski
Hereditary Cancer in Clinical Practice|September 13, 2013
Hereditary breast cancer: ever more pieces to the polygenic puzzleNatalia Bogdanova, Sonja Helbig, Thilo Dörk
Hereditary Cancer in Clinical Practice|January 16, 2016
Association of polymorphisms with a family history of cancer and the presence of germline mutations in the BRCA1/BRCA2 genesGabriela C Fernandes, Rodrigo A D Michelli, Cristovam Scapulatempo-Neto, et al.
Hereditary Cancer in Clinical Practice|January 27, 2018
Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindredsMev Dominguez-Valentin, D Gareth R Evans, Sigve Nakken, et al.
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