Symptomatic familial adenomatous polyposis in an adolescent: A case report
Author:
Publisher
Elsevier BV
Subject
Surgery
Reference20 articles.
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2. Hes FJ, Nielsen M, Bik EC, et al. Somatic APC mosaicism: an underestimated cause of polyposis coli. Gut. 2008; 57(1):71-76. doi:10.1136/gut.2006.117796.
3. Farinella E, Soobrah R, Phillips RKS, Clark SK. Familial adenomatous polyposis (FAP) and gender. Does gender influence the genetic transmission of FAP? Fam Cancer. 2010; 9(3):405-406. doi:10.1007/s10689-010-9341-x.
4. Cruz-Correa M, Giardiello FM. Diagnosis and management of hereditary colon cancer. Gastroenterol Clin North Am. 2002; 31(2):537-549, x. doi:10.1016/s0889-8553(02)00009-2.
5. Campos FG. Surgical treatment of familial adenomatous polyposis: dilemmas and current recommendations. World J Gastroenterol. 2014; 20(44):16620-16629. doi:10.3748/wjg.v20.i44.16620.
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