Hamartomatous Polyposis Syndromes
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-74259-5_13
Reference93 articles.
1. Schreibman IR, Baker M, Amos C, McGarrity TJ. The Hamartomatous polyposis syndromes - a clinical and molecular review. Am J Gastroenterol. 2005;100:476–90.
2. Ngeow J, Heald B, Rybicki LA, et al. Prevalence of germline PTEN, BMPR1A, SMAD4, STK11, and ENG mutations in patients with moderate-load colorectal polyps. Gastroenterology. 2013;144:1402–9. https://doi.org/10.1053/j.gastro.2013.02.001 .
3. Jelsig AM. Hamartomatous polyps – a clinical and molecular genetic study. Dan Med J. 2016. https://doi.org/10.1111/cge.12693 .
4. Aretz S. The differential diagnosis and surveillance of hereditary gastrointestinal polyposis syndromes. Dtsch Arztebl Int. 2010;107:163–73. https://doi.org/10.3238/arztebl.2010.0163 .
5. van Lier M, Wagner A, Mathus-Vliegen E, et al. High cancer risk in Peutz–Jeghers syndrome: a systematic review and surveillance recommendations. Am J Gastroenterol. 2010;105:1258–64. https://doi.org/10.1038/ajg.2009.725 .
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