Aarnio M, Sankila R, Pukkala E, Salovaara R, Aaltonen LA, de la Chapelle A, Peltomäki P, Mecklin JP, Järvinen HJ. Cancer risk in mutation carriers of DNA-mismatch-repair genes // Int J Cancer, 1999; 81:214-21810.1002/(SICI)1097-0215(19990412)81:2<214::AID-IJC8>3.0.CO;2-LSearch in Google Scholar

Barrow E, Robinson L, Alduaij W, Shenton A, Clancy T, Lalloo F, Hill J, Evans DG. Cumulative lifetime incidence of extracolonic cancers in Lynch syndrome: a report of 121 families with proven mutations // Clin Genet, 2009; 75(2):141-14910.1111/j.1399-0004.2008.01125.xSearch in Google Scholar

Bertario L, Russo A, Radice P, Varesco L, Eboli M, Spinelli P, Reyna A, Sala P. Genotype and phenotype factors as determinants for rectal stump cancer in patients with familial adenomatous polyposis. Hereditary Colorectal Tumors Registry // Ann Surg, 2000; 231:538-54310.1097/00000658-200004000-00013Search in Google Scholar

Boyle P and Ferlay J. Cancer incidence and mortality in Europe, 2004 // Ann Oncol, 2005; 16: 481-48810.1093/annonc/mdi098Search in Google Scholar

Church J, Burke C, MsGannon E, Pastean O, Clark B. Predicting polyposis severity by proctoscopy: how reliable is it? // Dis Colon Rectum, 2001; 44:1249-125410.1007/BF02234779Search in Google Scholar

Church J, Simmang C. Practice parameters for the treatment of patients with dominantly inherited colorectal cancer (familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer) // Dis Colon Rectum, 2003; 46:1001-101210.1007/s10350-004-7273-ySearch in Google Scholar

Giardiello FM, Brensinger JD, Luce MC, Petersen GM, Cayouette MC, Krush AJ, Bacon JA, Booker SV, Bufill JA, Hamilton SR. Phenotypic expression in adenomatous polyposis families with mutation in the 5' region of the adenomatous polyposis coli gene // Ann Intern Med 1997; 126:514-51910.7326/0003-4819-126-7-199704010-00003Search in Google Scholar

Goecke T, Schulmann K, Engel C, Holinski-Feder E, Pagenstecher C, Schackert HK, Kloor M, Kuntsmann E, Vogelsang H, Keller G, Dietmaier W, Mangold E et al. Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: A report by the German HNPCC Consortium // J Clin Oncol, 2006; 24:1-810.1200/JCO.2005.03.7333Search in Google Scholar

Guillem JG, Wood WC, Moley JF, Berchuck A, Karlan BY, Mutch DG, Gagel RF, Weitzel J, Morrow M, Weber BL, Giardiello F, Rodriguez-Bigas MA, Church J, Gruber S, Offit K. ASCO/SSO review of current role of risk-reducing surgery in common hereditary cancer syndromes // Ann Surg Oncol, 2006; 13:1296-132110.1245/s10434-006-9036-6Search in Google Scholar

Gylling AH, Nieminen TT, Abdel-Rahman WM, Nuorva K, Juhola M, Joensuu EI, Järvinen HJ, Mecklin JP, Aarnio M, Peltomäki PT. Differential cancer predisposition in Lynch syndrome: insights from molecular analysis of brain and urinary tract tumors // Carcinogenesis, 2008; 29(7):1351-135910.1093/carcin/bgn133Search in Google Scholar

Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, Nakagawa H, Sotamaa K, Prior TW, Westman J, Panescu J, Fix D, Lockman J, Comeras I, de la Chapelle A. Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer) // N Engl J Med, 2005; 352: 1851-186010.1056/NEJMoa043146Search in Google Scholar

Hampel H, Sweet K, Westman JA, Offit K, Eng C. Referral for cancer genetics consultation: a review and compilation of risk assessment criteria // J Med Genet, 2004; 41:81-9110.1136/jmg.2003.010918Search in Google Scholar

Koornstra JJ, Mourits MJ, Sijmons RH, Leliveld AM, Hollema H, Kleibeuker JH, Management of extracolonic tumours in patients with Lynch syndrome // Lancet Oncol, 2009; 10(4):400-40 Laken, S. J., Petersen, G. M., Gruber, S. B., Oddoux, C., Ostrer, H., Giardiello, F. M., Hamilton, S. R., Hampel, H., Markowitz, A., Klimstra, D., Jhanwar, S., Winawer, S., Offit, K., Luce, M. C., Kinzler, K. W., Vogelstein, B. Familial colorectal cancer in Askenazim due to a hypermutable tract in, A. P. C. // Nature Genet, 1997; 17:79-83Search in Google Scholar

Laurent-Puig P, Beroud C, Soussi T. APC gene: database of germline and somatic mutations in human tumors and cell lines // Nucl Acids Res, 1998; 26:269-27010.1093/nar/26.1.269Search in Google Scholar

Lee JS, Petrelli NJ, Rodrigues-Bigas MA. Rectal cancer in hereditary nonpolyposis colorectal cancer // Am J Surg, 2001; 181:207-21010.1016/S0002-9610(01)00568-2Search in Google Scholar

Lynch HT, de la Chapelle A. Hereditary colorectal cancer. N Engl J Med, 2003; 348(10):919-93210.1056/NEJMra012242Search in Google Scholar

Lynch HT, Shaw MW, Magnuson CW, Larsen AL, Krush AJ. Hereditary factors in two large midwestern kindreds // Arch Intern Med, 1996; 117:206-21210.1001/archinte.117.2.206Search in Google Scholar

Manchada R, Menon U, Michaelson-Cohen R, Beller U, Jacobs I. Hereditary non-polyposis colorectal cancer or Lynch syndrome: the gynaecological perspective // Curr Opin Obstet Gynecol, 2009; 21(1):31-3810.1097/GCO.0b013e32831c844dSearch in Google Scholar

Park YJ, Shin KH, Park JG. Risk of gastric cancer in hereditary nonpolyposis colorectal cancer in Korea // Clin Cancer Res, 2000; 6:2994-2998Search in Google Scholar

Sampson JR, Dolwani S, Jones S, Eccles D, Ellis A, Evans DG, Frayling I, Jordan S, Maher ER, Mak T, Maynard J, Pigatto F, Shaw J, Cheadle JP. Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH // Lancet, 2003; 362:39-4110.1016/S0140-6736(03)13805-6Search in Google Scholar

Scaife CL, Rodriguez-Bigas MA. Lynch syndrome: implications for the surgeon // Clin Colorectal Cancer, 2003; 3:92-9810.3816/CCC.2003.n.01512952564Search in Google Scholar

Sieber OM, Lipton L, Crabtree M, Heinimann K, Fidalgo P, Philipps RK, Bisgaard ML, Orntoft TF, Aaltonen LA, Hodgson SV, Thomas HJ, Tomlinson IP. Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH // N Engl J Med, 2003; 348(9):791-79910.1056/NEJMoa02528312606733Search in Google Scholar

Soravia C, Berk T, McLeod RS, Cohen Z. Desmoid disease in patients with familial adenomatous polyposis // Dis Colon Rectum, 2000; 43:363-36910.1007/BF02258303Search in Google Scholar

Spirio L, Olscwang S, Groden J, Robertson M, Samowitz W, Joslyn G, Gelbert L, Thliveris A, Carlson M, Otterud B et al. Alleles of the APC gene: an attenuated form of familial polyposis // Cell, 1993; 75:951-95710.1016/0092-8674(93)90538-2Search in Google Scholar

Tomlinson I, Rahman N, Frayling I, Mangion J, Barfoot R, Hamoudi R, Seal S, Northover J, Thomas HJ, Neale K, Hodgson S, Talbot I, Houlston R, Stratton MR. Inherited susceptibility to colorectal adenomas and carcinomas. Evidence for a new predisposition gene on 15q14-q22 // Gastroenterology, 1999; 116:789-795Search in Google Scholar

Trimbath JD, Giardiello FM. Review article: genetic testing and counselling for hereditary colorectal cancer // Aliment Pharmacol Ther, 2002; 16: 1843-185710.1046/j.1365-2036.2002.01357.xSearch in Google Scholar

Vasen HF, Nagengast FM, Khan PM. Interval cancers in hereditary non-polyposis colorectal cancer (Lynch syndrome) // Lancet, 1995; 345:1183-118410.1016/S0140-6736(95)91016-6Search in Google Scholar

Vasen HF, van der Luijt RB, Slors JF, Buskens E, de Ruiter P, Baeten CG, Schouten WR, Oostvogel HJ, Kuijpers JH, Tops CM, Meera Khan P. Molecular genetic tests as a guide to surgical management of familial adenomatous polyposis // Lancet, 1996; 348:433-43510.1016/S0140-6736(96)01340-2Search in Google Scholar

Watson P, Lynch HT. Extracolonic cancer in hereditary nonpolyposis colorectal cancer // Cancer, 1993; 71:677-68510.1002/1097-0142(19930201)71:3<677::AID-CNCR2820710305>3.0.CO;2-#Search in Google Scholar

Watson P, Vasen HF, Mecklin JP, Bernstein I, Aarnio M, Järvinen HJ, Myrhøj T, Sunde L, Wijnen JT, Lynch HT. The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome // Int J Cancer, 2008; 123(2): 444-44910.1002/ijc.23508Search in Google Scholar

eISSN:
1407-981X
ISSN:
1407-981X
Language:
English
Publication timeframe:
Volume Open
Journal Subjects:
Medicine, Clinical Medicine, Surgery, other