Broadening risk profile in familial colorectal cancer type X; increased risk for five cancer types in the national Danish cohort

Autor: Christina Therkildsen, Maria Rasmussen, Lars Smith-Hansen, Thomas Kallemose, Lars Joachim Lindberg, Mef Nilbert

Publikováno v: BMC Cancer, Vol 20, Iss 1, Pp 1-10 (2020)

Abstract Background Familial colorectal cancer type X (FCCTX) is a phenotypically defined subset of hereditary colorectal cancer with unknown and potentially heterogeneous genetic aetiology. FCCTX has been characterized as a colorectal cancer-specifi

Externí odkaz: https://doaj.org/article/7717eb3407c34a65b7fdbb3551613811

Broadening risk profile in familial colorectal cancer type X; increased risk for five cancer types in the national Danish cohort

Autor: Thomas Kallemose, Lars Smith-Hansen, Maria Rasmussen, Lars Joachim Lindberg, Christina Therkildsen, Mef Nilbert

Publikováno v: BMC Cancer, Vol 20, Iss 1, Pp 1-10 (2020)
Therkildsen, C, Rasmussen, M, Smith-Hansen, L, Kallemose, T, Lindberg, L J & Nilbert, M 2020, ' Broadening risk profile in familial colorectal cancer type X; increased risk for five cancer types in the national Danish cohort ', BMC Cancer, vol. 20, no. 1, 345 . https://doi.org/10.1186/s12885-020-06859-5
BMC Cancer

Background Familial colorectal cancer type X (FCCTX) is a phenotypically defined subset of hereditary colorectal cancer with unknown and potentially heterogeneous genetic aetiology. FCCTX has been characterized as a colorectal cancer-specific syndrom

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8da6a9af1abf1505eeefb736aa9882a
http://link.springer.com/article/10.1186/s12885-020-06859-5

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Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium 'Care for CMMR-D' (C4CMMR-D)

Autor: Jan Loeffen, G Sebille, Birgit Burkhardt, Martine Muleris, Olivier Caron, Franck Bourdeaut, Zeinab Ghorbanoghli, Chrystelle Colas, Denisa Ilencikova, Laurence Brugières, Christian P. Kratz, Alex Duval, Natacha Entz-Werle, Noémie Lavoine, Hans F. A. Vasen, Odile Cabaret, Yael Goldberg, Katharina Wimmer, Fred H. Menko

Publikováno v: Vasen, H F A, Ghorbanoghli, Z, Bourdeaut, F, Cabaret, O, Caron, O, Duval, A, Entz-Werle, N, Goldberg, Y, Ilencikova, D, Kratz, C P, Lavoine, N, Loeffen, J, Menko, F H, Muleris, M, Sebille, G, Colas, C, Burkhardt, B, Brugieres, L & Wimmer, K 2014, ' Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium "Care for CMMR-D" (C4CMMR-D) ', Journal of Medical Genetics, vol. 51, no. 5, pp. 283-293 . https://doi.org/10.1136/jmedgenet-2013-102238
Journal of Medical Genetics, 51(5), 283-293. BMJ Publishing Group
Journal of Medical Genetics, 51(5), 283-293

Lynch syndrome (LS) is an autosomal dominant disorder caused by a defect in one of the DNA mismatch repair genes: MLH1, MSH2, MSH6 and PMS2. In the last 15 years, an increasing number of patients have been described with biallelic mismatch repair gen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab1a204af594eff901b94e97089c571a
https://hdl.handle.net/1887/117380

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