1. Broadening the phenotypic spectrum of POP1‐skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasia. Issue 1 (22nd February 2017) Authors: Barraza‐García, J.; Rivera‐Pedroza, C.I.; Hisado‐Oliva, A.; Belinchón‐Martínez, A.; Sentchordi‐Montané, L.; Duncan, E.L.; Clark, G.R.; del Pozo, A.; Ibáñez‐Garikano, K.; Offiah, A.; Prieto‐Matos, P.; Cormier‐Daire, V.; Heath, K.E. Journal: Clinical genetics Issue: Volume 92:Issue 1(2017) Page Start: 91 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗