How to cite this article: Hempel M, Rivera Brugués N, Wagenstaller J, Lederer G, Weitensteiner A, Seidel H, Meitinger T, Strom TM. 2009. Microdeletion syndrome 16p11.2-p12.2: Clinical and molecular characterization. Am J Med Genet Part A 149A:2106–2112.
Microdeletion syndrome 16p11.2-p12.2: Clinical and molecular characterization†
Article first published online: 12 AUG 2009
Copyright © 2009 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 149A, Issue 10, pages 2106–2112, October 2009
How to Cite
Hempel, M., Rivera Brugués, N., Wagenstaller, J., Lederer, G., Weitensteiner, A., Seidel, H., Meitinger, T. and Strom, T. M. (2009), Microdeletion syndrome 16p11.2-p12.2: Clinical and molecular characterization. Am. J. Med. Genet., 149A: 2106–2112. doi: 10.1002/ajmg.a.33042
- Issue published online: 24 SEP 2009
- Article first published online: 12 AUG 2009
- Manuscript Accepted: 13 JUL 2009
- Manuscript Received: 5 MAR 2009
- NGFN. Grant Number: 01GS08163
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)
- 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!