How to cite this article: Carter MT, Picketts DJ, Hunter AG, Graham GE. 2009. Further clinical delineation of the Börjeson–Forssman–Lehmann syndrome in patients with PHF6 mutations. Am J Med Genet Part A 149A:246–250.
Further clinical delineation of the Börjeson–Forssman–Lehmann syndrome in patients with PHF6 mutations†
Version of Record online: 22 JAN 2009
Copyright © 2009 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 149A, Issue 2, pages 246–250, February 2009
How to Cite
Carter, M. T., Picketts, D. J., Hunter, A. G. and Graham, G. E. (2009), Further clinical delineation of the Börjeson–Forssman–Lehmann syndrome in patients with PHF6 mutations. Am. J. Med. Genet., 149A: 246–250. doi: 10.1002/ajmg.a.32624
- Issue online: 22 JAN 2009
- Version of Record online: 22 JAN 2009
- Manuscript Accepted: 18 SEP 2008
- Manuscript Received: 9 APR 2008
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!