Communicated by Peter J. Oefner
Deep intronic APC mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis†
Version of Record online: 16 APR 2012
© 2012 Wiley-Liss, Inc.
Volume 33, Issue 7, pages 1045–1050, July 2012
How to Cite
Spier, I., Horpaopan, S., Vogt, S., Uhlhaas, S., Morak, M., Stienen, D., Draaken, M., Ludwig, M., Holinski-Feder, E., Nöthen, M. M., Hoffmann, P. and Aretz, S. (2012), Deep intronic APC mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis. Hum. Mutat., 33: 1045–1050. doi: 10.1002/humu.22082
- Issue online: 5 JUN 2012
- Version of Record online: 16 APR 2012
- Accepted manuscript online: 19 MAR 2012 10:18AM EST
- Manuscript Accepted: 5 MAR 2012
- Manuscript Received: 21 NOV 2011
- German Cancer Aid (Deutsche Krebshilfe e.V. Bonn). Grant Number: 108421
Options for accessing this content:
- If you are a society or association member and require assistance with obtaining online access instructions please contact our Journal Customer Services team.
- If your institution does not currently subscribe to this content, please recommend the title to your librarian.
- Login via other institutional login options http://onlinelibrary.wiley.com/login-options.
- You can purchase online access to this Article for a 24-hour period (price varies by title)
- If you already have a Wiley Online Library or Wiley InterScience user account: login above and proceed to purchase the article.
- New Users: Please register, then proceed to purchase the article.
Login via OpenAthens
Search for your institution's name below to login via Shibboleth.
Registered Users please login:
- Access your saved publications, articles and searches
- Manage your email alerts, orders and subscriptions
- Change your contact information, including your password
Please register to:
- Save publications, articles and searches
- Get email alerts
- Get all the benefits mentioned below!