Conflict of interest: none.
Craniosynostosis and radial ray defect: A rare presentation of 22q11.2 deletion syndrome
Version of Record online: 27 JUN 2013
Copyright © 2013 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 8, pages 2024–2026, August 2013
How to Cite
2013. Craniosynostosis and radial ray defect: A rare presentation of 22q11.2 deletion syndrome. Am J Med Genet Part A. 161A:2024–2026., .
- Issue online: 24 JUL 2013
- Version of Record online: 27 JUN 2013
- Manuscript Accepted: 31 MAR 2013
- Manuscript Received: 23 JAN 2013
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