How to Cite this Article: van Kogelenberg M, Lerone M, De Toni T, Divizia MT, de Brouwer APM, Veltman JA, van Bokhoven H, Robertson SP. 2011. A novel Xp22.11 deletion causing a syndrome of craniosynostosis and periventricular nodular heterotopia. Am J Med Genet Part A 155: 3144–3147.
A novel Xp22.11 deletion causing a syndrome of craniosynostosis and periventricular nodular heterotopia†
Article first published online: 3 NOV 2011
Copyright © 2011 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 155, Issue 12, pages 3144–3147, December 2011
How to Cite
van Kogelenberg, M., Lerone, M., De Toni, T., Divizia, M. T., de Brouwer, A. P.M., Veltman, J. A., van Bokhoven, H. and Robertson, S. P. (2011), A novel Xp22.11 deletion causing a syndrome of craniosynostosis and periventricular nodular heterotopia. Am. J. Med. Genet., 155: 3144–3147. doi: 10.1002/ajmg.a.34311
- Issue published online: 21 NOV 2011
- Article first published online: 3 NOV 2011
- Manuscript Accepted: 6 AUG 2011
- Manuscript Received: 9 DEC 2010
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