Publication not explained
This publication has not yet been explained in plain language by the author(s). However, you can still read the publication.
If you are one of the authors, claim this publication so you can create a plain language summary to help more people find, understand and use it.
Featured Image
Read the Original
This page is a summary of: Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly, The American Journal of Human Genetics, July 2008, Elsevier,
DOI: 10.1016/j.ajhg.2008.05.012.
You can read the full text:
Contributors
The following have contributed to this page
