1. Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene. Issue 10 (1st October 2001) Authors: Mustapha, Myrna; Salem, Nabiha; Delague, Valérie; Chouery, Eliane; Ghassibeh, Michella; Rai, Myriam; Loiselet, Jacques; Petit, Christine; Mégarbané, André Journal: Journal of medical genetics Issue: Volume 38:Issue 10(2001) Page Start: e36 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗