|  Help  |  About  |  Contact Us

Publication : Mutations in MEOX1, encoding mesenchyme homeobox 1, cause Klippel-Feil anomaly.

First Author  Mohamed JY Year  2013
Journal  Am J Hum Genet Volume  92
Issue  1 Pages  157-61
PubMed ID  23290072 Mgi Id 
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

1 Bio Entities

Trail: Publication

0 Expression