Azadegan-Dehkordi, F., Bahrami, T., Shirzad, M., Karbasi, G., Yazdanpanahi, N., Farrokhi, E., . . . Hashemzadeh-Chaleshtori, M. (2019). Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran. J Audiol Otol.

Azadegan-Dehkordi, Fatemeh, Tayyebe Bahrami, Maryam Shirzad, Gelareh Karbasi, Nasrin Yazdanpanahi, Effat Farrokhi, Mahbobeh Koohiyan, Mohammad Amin Tabatabaiefar, and Morteza Hashemzadeh-Chaleshtori. "Mutations in GJB2 As Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of C.299-300delAT Mutation in Kurdish Population of Iran." J Audiol Otol 2019.

Azadegan-Dehkordi, Fatemeh, et al. "Mutations in GJB2 As Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of C.299-300delAT Mutation in Kurdish Population of Iran." J Audiol Otol 2019.