1. A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephaly. Issue 5 (May 1997) Authors: Steinberger, D; Collmann, H; Schmalenberger, B; Müller, U Journal: Journal of medical genetics Issue: Volume 34:Issue 5(1997) Page Start: 420 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗