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Mutation spectrum in South American Lynch syndrome families.
Dominguez-Valentin M, Nilbert M, Wernhoff P, López-Köstner F, Vaccaro C, Sarroca C, Palmero EI, Giraldo A, Ashton-Prolla P, Alvarez K, Ferro A, Neffa F, Caris J, Carraro DM, Rossi BM. Dominguez-Valentin M, et al. Among authors: ferro a. Hered Cancer Clin Pract. 2013 Dec 18;11(1):18. doi: 10.1186/1897-4287-11-18. Hered Cancer Clin Pract. 2013. PMID: 24344984 Free PMC article.
MLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome.
Dominguez-Valentin M, Wernhoff P, Cajal AR, Kalfayan PG, Piñero TA, Gonzalez ML, Ferro A, Sammartino I, Causada Calo NS, Vaccaro CA. Dominguez-Valentin M, et al. Among authors: ferro a. Front Oncol. 2016 Aug 24;6:189. doi: 10.3389/fonc.2016.00189. eCollection 2016. Front Oncol. 2016. PMID: 27606285 Free PMC article. No abstract available.
[Founder mutation in Lynch syndrome].
Cajal AR, Piñero TA, Verzura A, Santino JP, Solano AR, Kalfayan PG, Ferro A, Vaccaro C. Cajal AR, et al. Among authors: ferro a. Medicina (B Aires). 2016;76(3):180-2. Medicina (B Aires). 2016. PMID: 27295708 Free article. Spanish.
985 results