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Year Number of Results
2012 1
2013 1
2014 1
2015 1
2016 2
2018 1
2021 2
2022 1
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Page 1
[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. Medicina (B Aires). 2016;76(3):180-2. Medicina (B Aires). 2016. PMID: 27295708 Free article. Spanish.
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: cajal ar. 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.