Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly
Open Access
- 5 June 2008
- journal article
- research article
- Published by Elsevier
- Vol. 83 (1) , 18-29
- https://doi.org/10.1016/j.ajhg.2008.05.012
Abstract
No abstract availableKeywords
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