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Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity.
Parsons MT, Whiley PJ, Beesley J, Drost M, de Wind N, Thompson BA, Marquart L, Hopper JL, Jenkins MA; Australasian Colorectal Cancer Family Registry; Brown MA, Tucker K, Warwick L, Buchanan DD, Spurdle AB. Parsons MT, et al. Mol Carcinog. 2015 Jul;54(7):513-22. doi: 10.1002/mc.22116. Epub 2013 Dec 2. Mol Carcinog. 2015. PMID: 24302565 Free PMC article.
Cancer risk in 348 French MSH2 or MLH1 gene carriers.
Parc Y, Boisson C, Thomas G, Olschwang S. Parc Y, et al. J Med Genet. 2003 Mar;40(3):208-13. doi: 10.1136/jmg.40.3.208. J Med Genet. 2003. PMID: 12624141 Free PMC article. No abstract available.
Screening for Lynch syndrome in colorectal cancer: are we doing enough?
Canard G, Lefevre JH, Colas C, Coulet F, Svrcek M, Lascols O, Hamelin R, Shields C, Duval A, Fléjou JF, Soubrier F, Tiret E, Parc Y. Canard G, et al. Ann Surg Oncol. 2012 Mar;19(3):809-16. doi: 10.1245/s10434-011-2014-7. Epub 2011 Aug 31. Ann Surg Oncol. 2012. PMID: 21879275