References
Fretwell V, Rooney P (2014) Letter to the editor: rectal cancer in a 15-year-old with a novel MLH1 and MSH6 biallelic inheritance. Int J Colorectal Dis 30:435–436
Schwab M (ed) (2011) Encyclopedia of cancer, 3rd edn. Springer, Berlin, Heidelberg, 290p
Wimmer K, Kratz CP, Vasen HF, Caron O, Colas C, Entz-Werle N, Gerdes AM, Goldberg Y, Ilencikova D, Muleris M, Dival A, Lavoine N, Ruiz-Ponte C, Slavc I, Burkhardt B, Brugieres L, EU-Consortioum Care for CMMRD (C4CMMRD) (2014) Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium “care for CMMRD” (C4CMMRD). J Med Genet 51(6):35–365
Lavie O, Narod S, Lejbkowicz F, Dishon S, Goldberg Y, Gemer O, Rennert G (2011) Double heterozygosity in the BRCA1 and BRCA2 genes in the Jewish population. Ann Oncol 22(4):964–966
Gong P, Charles S, Rosenblum N, Wang Z, Witkiewicz AK (2012) A case of endometrial cancer in the context of a BRCA2 mutation and double heterozygosity for Lynch syndrome. Gynecol Oncol Case Rep 2(3):69–72
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Jasperson, K., Ballinger, L. Letter to the editor: mistaken inheritance. Int J Colorectal Dis 31, 711–712 (2016). https://doi.org/10.1007/s00384-015-2204-z
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DOI: https://doi.org/10.1007/s00384-015-2204-z