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Incidence of BRCA1 and BRCA2 mutations in 54 Chilean families with breast/ovarian cancer, genotype-phenotype correlations.
Gallardo M, Silva A, Rubio L, Alvarez C, Torrealba C, Salinas M, Tapia T, Faundez P, Palma L, Riccio ME, Paredes H, Rodriguez M, Cruz A, Rousseau C, King MC, Camus M, Alvarez M, Carvallo P. Gallardo M, et al. Among authors: camus m. Breast Cancer Res Treat. 2006 Jan;95(1):81-7. doi: 10.1007/s10549-005-9047-1. Epub 2005 Oct 27. Breast Cancer Res Treat. 2006. PMID: 16261400
[Treatment results of early breast cancer: a retrospective review].
Sánchez C, Bustos M, Camus M, Alvarez M, Goñi I, León A, Besa de C P. Sánchez C, et al. Among authors: camus m. Rev Med Chil. 2007 Apr;135(4):427-35. doi: 10.4067/s0034-98872007000400003. Epub 2007 May 16. Rev Med Chil. 2007. PMID: 17554450 Free article. Spanish.
BRCA1 and BRCA2 founder mutations account for 78% of germline carriers among hereditary breast cancer families in Chile.
Alvarez C, Tapia T, Perez-Moreno E, Gajardo-Meneses P, Ruiz C, Rios M, Missarelli C, Silva M, Cruz A, Matamala L, Carvajal-Carmona L, Camus M, Carvallo P. Alvarez C, et al. Among authors: camus m. Oncotarget. 2017 Jun 29;8(43):74233-74243. doi: 10.18632/oncotarget.18815. eCollection 2017 Sep 26. Oncotarget. 2017. PMID: 29088781 Free PMC article.
645 results