1. Autosomal recessive congenital cataract, intellectual disability phenotype linked to STX3 in a consanguineous Tunisian family. (30th October 2014) Authors: Chograni, M.; Alkuraya, F.S.; Ourteni, I.; Maazoul, F.; Lariani, I.; Chaabouni, H.B. Journal: Clinical genetics Issue: Volume 88:Number 3(2015:Sep.) Page Start: 283 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical and genetic characterization of Bardet–Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis. (5th April 2013) Authors: M'hamdi, O.; Redin, C.; Stoetzel, C.; Ouertani, I.; Chaabouni, M.; Maazoul, F.; M'rad, R.; Mandel, J.L.; Dollfus, H.; Muller, J.; Chaabouni, H. Journal: Clinical genetics Issue: Volume 85:Number 2(2014:Feb.) Page Start: 172 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗