These two authors contributed equally to this work.
CHD7 mutations causing CHARGE syndrome are predominantly of paternal origin
Version of Record online: 27 MAY 2011
© 2011 John Wiley & Sons A/S
Volume 81, Issue 3, pages 234–239, March 2012
How to Cite
Pauli, S., von Velsen, N., Burfeind, P., Steckel, M., Mänz, J., Buchholz, A., Borozdin, W. and Kohlhase, J. (2012), CHD7 mutations causing CHARGE syndrome are predominantly of paternal origin. Clinical Genetics, 81: 234–239. doi: 10.1111/j.1399-0004.2011.01701.x
- Issue online: 31 JAN 2012
- Version of Record online: 27 MAY 2011
- Accepted manuscript online: 7 MAY 2011 03:58AM EST
- Received 15 March 2011, revised and accepted for publication 2 May 2011
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!
Patients and/or caregivers may access this content for use in relation to their own personal healthcare or that of a family member only. Terms and conditions will apply.