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Familial Cancer|March 16, 2011
Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studiesKarin Hardt, Sven Boris Heick, Beate Betz, et al.Familial Cancer|June 15, 2011
Familial colorectal cancer: eleven years of data from a registry program in SwitzerlandMichal Kovac, Endre Laczko, Ritva Haider, et al.Familial Cancer|June 18, 2011
Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individualsMev Dominguez Valentin, Felipe Carneiro da Silva, Erika Maria Monteiro dos Santos, et al.Familial Cancer|June 18, 2011
Communication of BRCA1 and BRCA2 genetic test results to health care providers following genetic testing at a tertiary care centerK Ready, B K Arun, K M Schmeler, et al.Familial Cancer|June 23, 2011
Factors affecting encouragement of relatives among families with Lynch syndrome to seek medical assessmentNoriko Ishii, Masami Arai, Yurie Koyama, et al.Familial Cancer|January 1, 2017
Novel and reported pathogenic variants in exon 11 of BRCA2 gene in a cohort of Sri Lankan young breast cancer patientsSumadee De Silva, Kamani Hemamala Tennekoon, Aravinda Dissanayake, et al.Familial Cancer|April 15, 2014
BRCA1 point mutations in premenopausal breast cancer patients from Central SudanIda Biunno, Gitana Aceto, Khalid Dafaallah Awadelkarim, et al.Familial Cancer|May 1, 2014
Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignanciesR Renella, J Carnevale, K A Schneider, et al.Familial Cancer|April 29, 2014
BRCA1 founder mutations compared to ovarian cancer in BelarusAlena Savanevich, Oleg Oszurek, Jan Lubiński, et al.Familial Cancer|June 12, 2012
Causes of death of mutation carriers in Finnish Lynch syndrome familiesKirsi Pylvänäinen, Tuula Lehtinen, Ilmo Kellokumpu, et al.Pageof 151