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                                       Details for article 18 of 27 found articles
 
 
  Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly
 
 
Title: Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly
Author: Roessler, Erich
Ouspenskaia, Maia V.
Karkera, Jayaprakash D.
Vélez, Jorge I.
Kantipong, Amy
Lacbawan, Felicitas
Bowers, Peter
Belmont, John W.
Towbin, Jeffrey A.
Goldmuntz, Elizabeth
Feldman, Benjamin
Muenke, Maximilian
Appeared in: The American journal of human genetics
Paging: Volume 83 (2008) nr. 1 pages 12 p.
Year: 2008
Contents:
Publisher: The American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 18 of 27 found articles
 
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