1. Non-syndromic severe hypodontia caused by a novel frameshift insertion mutation in the homeobox of the MSX1 gene. (March 2017) Authors: Abid, Mushriq F.; Simpson, M.A.; Petridis, Christos; Cobourne, M.T.; Sharpe, P.T. Journal: Archives of oral biology Issue: Volume 75(2017) Page Start: 8 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗