1. A large multiexonic genomic deletion within the ALMS1 gene causes Alström syndrome in a consanguineous Pakistani family. Issue 4 (18th August 2015) Authors: Nikopoulos, K.; Butt, G. U.; Farinelli, P.; Mudassar, M.; Domènech‐Estévez, E.; Samara, C.; Kausar, M.; Masroor, I.; Chrast, R.; Rivolta, C.; Siddiqi, S. Journal: Clinical genetics Issue: Volume 89:Issue 4(2016) Page Start: 510 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗