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Mutations of hMLH1 and hMSH2 in patients with suspected hereditary nonpolyposis colorectal cancer: correlation with microsatellite instability and abnormalities of mismatch repair protein expression.
Scartozzi M, Bianchi F, Rosati S, Galizia E, Antolini A, Loretelli C, Piga A, Bearzi I, Cellerino R, Porfiri E. Scartozzi M, et al. Among authors: porfiri e. J Clin Oncol. 2002 Mar 1;20(5):1203-8. doi: 10.1200/JCO.2002.20.5.1203. J Clin Oncol. 2002. PMID: 11870161
Assessing the pathogenicity of MLH1 missense mutations in patients with suspected hereditary nonpolyposis colorectal cancer: correlation with clinical, genetic and functional features.
Belvederesi L, Bianchi F, Loretelli C, Gagliardini D, Galizia E, Bracci R, Rosati S, Bearzi I, Viel A, Cellerino R, Porfiri E. Belvederesi L, et al. Among authors: porfiri e. Eur J Hum Genet. 2006 Jul;14(7):853-9. doi: 10.1038/sj.ejhg.5201628. Epub 2006 May 17. Eur J Hum Genet. 2006. PMID: 16724012
MSH2 splice site mutation and endometrial cancer.
Bianchi F, Rosati S, Belvederesi L, Loretelli C, Catalani R, Mandolesi A, Bracci R, Bearzi I, Porfiri E, Cellerino R. Bianchi F, et al. Among authors: porfiri e. Int J Gynecol Cancer. 2006 May-Jun;16(3):1419-23. doi: 10.1111/j.1525-1438.2006.00572.x. Int J Gynecol Cancer. 2006. PMID: 16803540
74 results