Conflict of interest: none.
Expanding the SHOC2 mutation associated phenotype of noonan syndrome with loose anagen hair: Structural brain anomalies and myelofibrosis
Version of Record online: 5 AUG 2013
Copyright © 2013 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 10, pages 2420–2430, October 2013
How to Cite
2013. Expanding the SHOC2 mutation associated phenotype of noonan syndrome with loose anagen hair: Structural brain anomalies and myelofibrosis. Am J Med Genet Part A 161A:2420–2430., , , , , , , , , .
- Issue online: 17 SEP 2013
- Version of Record online: 5 AUG 2013
- Manuscript Accepted: 31 MAY 2013
- Manuscript Received: 15 FEB 2013
- National Institute of General Medical Sciences. Grant Number: 8P20GM103464-08
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