How to cite this article: Suri M, Kelehan P, O'Neill D, Vadeyar S, Grant J, Ahmed SF, Tolmie J, McCann E, Lam W, Smith S, FitzPatrick D, Hastie ND, Reardon W. 2007. WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations. Am J Med Genet Part A 143A:2312–2320.
WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations†
Article first published online: 12 SEP 2007
Copyright © 2007 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 143A, Issue 19, pages 2312–2320, 1 October 2007
How to Cite
Suri, M., Kelehan, P., O'Neill, D., Vadeyar, S., Grant, J., Ahmed, S. F., Tolmie, J., McCann, E., Lam, W., Smith, S., FitzPatrick, D., Hastie, N. D. and Reardon, W. (2007), WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations. Am. J. Med. Genet., 143A: 2312–2320. doi: 10.1002/ajmg.a.31924
- Issue published online: 24 SEP 2007
- Article first published online: 12 SEP 2007
- Manuscript Accepted: 26 MAY 2007
- Manuscript Received: 15 JUN 2006
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