How to Cite this Article: Harrison V, Connell L, Hayesmoore J, McParland J, Pike MG, Blair E. 2011. Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters. Am J Med Genet Part A 155: 2826–2831.
Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters†
Article first published online: 30 SEP 2011
Copyright © 2011 Wiley-Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 155, Issue 11, pages 2826–2831, November 2011
How to Cite
Harrison, V., Connell, L., Hayesmoore, J., McParland, J., Pike, M. G. and Blair, E. (2011), Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters. Am. J. Med. Genet., 155: 2826–2831. doi: 10.1002/ajmg.a.34255
- Issue published online: 20 OCT 2011
- Article first published online: 30 SEP 2011
- Manuscript Accepted: 20 JUL 2011
- Manuscript Received: 4 MAR 2011
Options for accessing this content:
- If you have access to this content through a society membership, please first log in to your society website.
- If you would like institutional access 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!