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WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations

Suri, M. et al. (2007) WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations. American Journal of Medical Genetics Part A, 143A, pp. 2312-2320.

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Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Ahmed, Dr Syed and Ahmed, Professor Syed Faisal
Authors: Suri, M., Kelehan, P., O'Neill, D., Vadeyar, S., Grant, J., Ahmed, S., Ahmed, S., Tolmie, J., McCann, E., Lam, W., Smith, S., FitzPatrick, D., Hastie, N., and Reardon, W.
College/School:College of Medical Veterinary and Life Sciences
Journal Name:American Journal of Medical Genetics Part A

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