APC gene mutations causing familial adenomatous polyposis in Polish patients
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF03195640.pdf
Reference51 articles.
1. Aretz S, Stienen D, Uhlhaas S, Pagenstecher C, Mangold E, Caspari R, et al. 2005. Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis. J Med Genet 42: 185–192.
2. Bjork J, Akerbrant H, Iselius L, Bergman A, Engwall Y, Wahlstrom J, et al. 2001. Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: cumulative risks and APC gene mutations. Gastroenterology 121: 1127–1135.
3. Brozek I, Plawski A, Podralska M, Kanka C, Slomski R, Limon J, 2008. Thyroid cancer in two siblings with FAP syndrome and APC mutation. Int J Colorectal Dis 23: 331–332.
4. Cetta F, Dhamo A, 2007. Inherited multitumoral syndromes including colorectal carcinoma. Surg Oncol 16 Suppl 1: S17–23.
5. Chen CS, Phillips KD, Grist S, Bennet G, Craig JE, Muecke JS, Suthers GK, 2006. Congenital hypertrophy of the retinal pigment epithelium, CHRPE. in familial colorectal cancer. Fam Cancer 5: 397–404.
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