How to Cite this Article: Stevens SJC, van Ravenswaaij-Arts CMA, Janssen JWH, Klein Wassink-Ruiter JS, van Essen AJ, Dijkhuizen T, van Rheenen J, Heuts-Vijgen R, Stegmann APA, Smeets EEJGL, Engelen JJM. 2011. MYT1L is a candidate gene for intellectual disability in patients with 2p25.3 (2pter) deletions. Am J Med Genet Part A 155: 2739–2745.
MYT1L is a candidate gene for intellectual disability in patients with 2p25.3 (2pter) deletions†
Article first published online: 11 OCT 2011
Copyright © 2011 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 155, Issue 11, pages 2739–2745, November 2011
How to Cite
Stevens, S. J.C., van Ravenswaaij-Arts, C. M.A., Janssen, J. W.H., Klein Wassink-Ruiter, J. S., van Essen, A. J., Dijkhuizen, T., van Rheenen, J., Heuts-Vijgen, R., Stegmann, A. P.A., Smeets, E. E.J.G.L. and Engelen, J. J.M. (2011), MYT1L is a candidate gene for intellectual disability in patients with 2p25.3 (2pter) deletions. Am. J. Med. Genet., 155: 2739–2745. doi: 10.1002/ajmg.a.34274
- Issue published online: 20 OCT 2011
- Article first published online: 11 OCT 2011
- Manuscript Accepted: 28 JUL 2011
- Manuscript Received: 17 FEB 2011
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