Hereditäre kolorektale Karzinogenese
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pathology and Forensic Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00292-023-01200-w.pdf
Reference20 articles.
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2. Aronson M, Colas C, Shuen A, Hampel H, Foulkes WD, Feldman BH, Goldberg Y, Muleris M, Wolfe Schneider K, McGee RB, Jasperson K, Rangaswami A, Brugieres L, Tabori U (2022) Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD): recommendations from the international consensus working group. J Med Genet 59(4):318–327. https://doi.org/10.1136/jmedgenet-2020-107627
3. Bläker H, Haupt S, Morak M, Holinski-Feder E, Arnold A, Horst D, Sieber-Frank J, Seidler F, von Winterfeld M, Alwers E, Chang-Claude J, Brenner H, Roth W, Engel C, Löffler M, Möslein G, Schackert H‑K, Weitz J, Perne C, Aretz S, Hüneburg R, Schmiegel W, Vangala D, Rahner N, Steinke-Lange V, Heuveline V, von Knebel Doeberitz M, Ahadova A, Hoffmeister M, Kloor M (2020) Age-dependent performance of BRAF mutation testing in Lynch syndrome diagnostics. Int J Cancer 147(10):2801–2810. https://doi.org/10.1002/ijc.33273
4. Buchanan DD, Stewart JR, Clendenning M, Rosty C, Mahmood K, Pope BJ, Jenkins MA, Hopper JL, Southey MC, Macrae FA, Winship IM, Win AK (2018) Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1. Genet Med 20(8):890–895. https://doi.org/10.1038/gim.2017.185
5. Da Weren R, Ligtenberg MJ, van Geurts Kessel A, de Voer RM, Hoogerbrugge N, Kuiper RP (2018) NTHL1 and MUTYH polyposis syndromes: two sides of the same coin? J Pathol 244(2):135–142. https://doi.org/10.1002/path.5002
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