Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid.

Kathrin Laue,Hans-Martin Pogoda,P. Daniel,A. van Haeringen,Y. Alanay,Simon von Ameln,Martin Rachwalski,Tim Morgan,M. Gray,M. Breuning,G. M. Sawyer,A. Sutherland-Smith,P. Nikkels,C. Kubisch,W. Bloch,B. Wollnik,M. Hammerschmidt,S. Robertson

Published 2011 in American Journal of Human Genetics

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