Chebly, A., Corbani, S., Abou Ghoch, J., Mehawej, C., Megarbane, A., & Chouery, E. (2018). First molecular study in Lebanese patients with Cockayne syndrome and report of a novel mutation in ERCC8 gene. BMC Med Genet.

Chebly, Alain, Sandra Corbani, Joelle Abou Ghoch, Cybel Mehawej, André Megarbane, and Eliane Chouery. "First Molecular Study in Lebanese Patients With Cockayne Syndrome and Report of a Novel Mutation in ERCC8 Gene." BMC Med Genet 2018.

Chebly, Alain, et al. "First Molecular Study in Lebanese Patients With Cockayne Syndrome and Report of a Novel Mutation in ERCC8 Gene." BMC Med Genet 2018.