Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (26) GO Terms (2) Nucleotides (57) Proteins (38) Interactants (155) Wiki
XB--481783

Papers associated with gdf5 (and Disease Ontology)



Limit to papers also referencing gene:
Show all gdf5 papers

Results 1 - 1 of 1 results

Page(s): 1

Sort Newest To Oldest Sort Oldest To Newest

Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome., Hempel A, Pagnamenta AT, Blyth M, Mansour S, McConnell V, Kou I, Ikegawa S, Tsurusaki Y, Matsumoto N, Lo-Castro A, Plessis G, Albrecht B, Battaglia A, Taylor JC, Howard MF, Keays D, Sohal AS, [Organization not found], Kühl SJ, Kühl SJ, Kini U, McNeill A., J Med Genet. March 1, 2016; 53 (3): 152-62.          

Page(s): 1