1. Improving detection and genetic counseling in carriers of spinal muscular atrophy with two copies of the SMN1 gene. (16th July 2013) Authors: Alías, L.; Barceló, M.J.; Bernal, S.; Martínez‐Hernández, R.; Also‐Rallo, E.; Vázquez, C.; Santana, A.; Millán, J.M.; Baiget, M.; Tizzano, E.F. Journal: Clinical genetics Issue: Volume 85:Number 5(2014:May) Page Start: 470 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗