Familial Adenomatous Polyposis
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-62345-6_5074
Reference10 articles.
1. Aihara, H., & Thompson, C. (2014). Diagnosis, surveillance, and treatment strategies for familial adenomatous polyposis: rationale and update. European Journal of Gastroenterology & Hepatology, 26(3), 255–262.
2. Basso, G., & Laghi, L. (2017). Hereditary or sporadic polyposis syndromes. Best Practice and Research: Clinical Gastroenterology, 31(4), 409–417.
3. Bellone, S., & Masserdotti, A. (2017). Polymerase epsilon (POLE) ultra-mutation in uterine tumors correlates with T lymphocyte infiltration and increased resistance to platinum-based chemotherapy in vitro. Gynecologic Oncology, 144, 146–152.
4. Dinarvand, P., & Guzman, M. D. (2019). Familial adenomatous polyposis syndrome: An update and review of extraintestinal manifestations. Archives of Pathology & Laboratory Medicine, 143, 1382–1398.
5. Half, E., Bercovich, D., & Rozen, P. (2009). Familial adenomatous polyposis. Orphanet Journal of Rare Diseases, 4, 222–223.
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