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36.  Umar A, Boland CR, Terdiman JP, Syngal S, de la Chapelle A, Rüschoff J, et al. Revised
                  Bethesda  Guidelines  for  hereditary  nonpolyposis  colorectal  cancer  (Lynch  syndrome)  and

                  microsatellite instability. J Natl Cancer Inst. 2004;96:261-8.

                         37.  Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, et al. Feasibility of
                  screening for Lynch syndrome among patients with colorectal cancer. J Clin Oncol. 2008;26:5783-8.

                         38.  Puangsricharoen  P,  Manchana  T,  Ariyasriwatana  C,  Triratanachat  S.

                  Immunohistochemistry staining for the mismatch repair proteins in endometrial cancer patients.
                  Thai J Obstet Gynaecol. 2020;28:79-85.

                         39.  Pilarski R, Burt R, Kohlman W, Pho L, Shannon KM, Swisher E. Cowden syndrome and

                  the PTEN hamartoma tumor syndrome: systematic review and revised diagnostic criteria. J Natl
                  Cancer Inst. 2013;105:1607-16.

                         40.  Beggs AD, Latchford AR, Vasen HF, Moslein G, Alonso A, Aretz S, et al. Peutz-Jeghers

                  syndrome: a systematic review and recommendations for management. Gut. 2010;59:975-86.
                         41.  Masciari S, Dillon DA, Rath M, Robson M, Weitzel JN, Balmana J, et al. Breast cancer

                  phenotype in women with TP53 germline mutations: a Li-Fraumeni syndrome consortium effort.

                  Breast Cancer Res Treat. 2012;133:1125-30.
                         42.  Kamihara J, Rana HQ, Garber JE. Germline TP53 mutations and the changing landscape

                  of Li-Fraumeni syndrome. Hum Mutat. 2014;35:654-62.

                         43.  Bougeard G, Renaux-Petel M, Flaman JM, Charbonnier C, Fermey P, Belotti M, et al.
                  Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers. J Clin Oncol. 2015;33:2345-52.

                         44.  Gonzalez KD, Noltner KA, Buzin CH, Gu D, Wen-Fong CY, Nguyen VQ, et al. Beyond Li

                  Fraumeni Syndrome: clinical characteristics of families with p53 germline mutations. J Clin Oncol.
                  2009;27:1250-6.

                         45.  Chompret  A,  Abel  A,  Stoppa-Lyonnet  D,  Brugiéres  L,  Pagés  S,  Feunteun  J,  et  al.

                  Sensitivity and predictive value of criteria for p53 germline mutation screening. J Med Genet.
                  2001;38:43-7.

                         46.  van der Post RS, Vogelaar IP, Carneiro F, Guilford P, Huntsman D, Hoogerbrugge N, et

                  al. Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline
                  CDH1 mutation carriers. J Med Genet. 2015;52:361-74.






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