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Familial Cancer|September 16, 2011
Low prevalence of BRCA1 and BRCA2 mutations in the sporadic breast cancer of Spanish populationInmaculada de Juan Jiménez, Eva Esteban Cardeñosa, Sarai Palanca Suela, et al.Familial Cancer|May 27, 2011
The liver: another organ involved in Muir Torre syndrome?F Morando, M Alaibac, A Romano, et al.Familial Cancer|April 20, 2011
Gastrointestinal polyps and cancer in Peutz-Jeghers syndrome: clinical aspectsA R Latchford, R K S PhillipsFamilial 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.Pageof 152