Author:
Dominguez-Valentin Mev,Nilbert Mef,Wernhoff Patrik,López-Köstner Francisco,Vaccaro Carlos,Sarroca Carlos,Palmero Edenir Ines,Giraldo Alejandro,Ashton-Prolla Patricia,Alvarez Karin,Ferro Alejandra,Neffa Florencia,Caris Junea,Carraro Dirce M,Rossi Benedito M
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Oncology
Reference30 articles.
1. Plazzer JP, Sijmons RH, Woods MO, Peltomaki P, Thompson B, DenDunnen JT, Macrae F: The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome. Fam Cancer 2013, 12: 175–180. 10.1007/s10689-013-9616-0
2. Giraldo A, Gomez A, Salguero G, Garcia H, Aristizabal F, Gutierrez O, Angel LA, Padron J, Martinez C, Martinez H, et al.: MLH1 and MSH2 mutations in Colombian families with hereditary nonpolyposis colorectal cancer (Lynch syndrome)–description of four novel mutations. Fam Cancer 2005, 4: 285–290. 10.1007/s10689-005-4523-7
3. Valentin MD, da Silva FC, dos Santos EM, Lisboa BG, de Oliveira LP, Ferreira Fde O, Gomy I, Nakagawa WT, Aguiar Junior S, Redal M, et al.: Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individuals. Fam Cancer 2011, 10: 641–647. 10.1007/s10689-011-9461-y
4. Sarroca C, Valle AD, Fresco R, Renkonen E, Peltomaki P, Lynch H: Frequency of hereditary non-polyposis colorectal cancer among Uruguayan patients with colorectal cancer. Clin Gen 2005, 68: 80–87. 10.1111/j.1399-0004.2005.00458.x
5. Rossi BM, Lopes A, Oliveira Ferreira F, Nakagawa WT, Napoli Ferreira CC, Casali Da Rocha JC, Simpson CC, Simpson AJ: hMLH1 and hMSH2 gene mutation in Brazilian families with suspected hereditary nonpolyposis colorectal cancer. Ann Surg Oncol 2002, 9: 555–561.
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