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Guidelines for the clinical management of familial adenomatous polyposis (FAP)

✍ Scribed by Vasen, H. F.A. (author);Möslein, G. (author);Alonso, A. (author);Aretz, S. (author);Bernstein, I. (author);Bertario, L. (author);Blanco, I. (author);Bülow, S. (author);Burn, J. (author);Capella, G. (author);Colas, C. (author);Engel, C. (author);Frayling, I. (author);Friedl, W. (author);Hes, F. J. (author);Hodgson, S. (author);Järvinen, H. (author);Mecklin, J. P. (author);Møller, P. (author);Myrhøi, T. (author);Nagengast, F. M. (author);Pare, Y. (author);Phillips, R. (author);Clark, S. K. (author);Ponz De Leon, M. (author);Renkonen-Sinisalo, L. (author);Sampson, J. R. (author);Stormorken, A. (author);Tejpar, S. (author);Thomas, H. J.W. (author);Wijnen, J. (author)

Book ID
125432433
Publisher
BMJ Publishing Group
Year
2008
Tongue
English
Weight
656 KB
Volume
57
Category
Article
ISSN
0017-5749

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Mutation analysis of the adenomatous polyposis coli (APC) gene in Danish patients with familial adenomatous polyposis (FAP)
✍ Marie Luise Bisgaard; RASMUS S. Ripa; Steffen Bülow 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 26 KB 👁 2 views

## Development of one hundred or more adenomas in the colon and rectum is diagnostic for the dominantly inherited, autosomal disease Familial Adenomatous Polyposis (FAP). It is possible to identify a mutation in the Adenomatous Polyposis Coli (APC) gene in approximately 80% of the patients, and alm