1. GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants. (April 2018) Authors: Koohiyan, Mahbobeh; Hashemzadeh-Chaleshtori, Morteza; Salehi, Mansoor; Abtahi, Hamidreza; Reiisi, Somayeh; Pourreza, Mohammad Reza; Noori-Daloii, Mohammad Reza; Tabatabaiefar, Mohammad Amin Journal: International journal of pediatric otorhinolaryngology Issue: Volume 107(2018:Apr.) Page Start: 121 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. GJB2‐related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations. (11th September 2019) Authors: Koohiyan, Mahbobeh; Koohian, Farideh; Azadegan‐Dehkordi, Fatemeh Journal: Annals of human genetics Issue: Volume 84:Number 2(2020:Mar.) Page Start: 107 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. The Radioprotective Effect of Ascorbic Acid and Kefir against Genotoxicity Induced by Exposure in Mice Blood Lymphocytes. (16th March 2021) Authors: Koohian, Farideh; Shahbazi-Gahrouei, Daryoush; Koohiyan, Mahbobeh; Shanei, Ahmad Journal: Nutrition and cancer Issue: Volume 73:Number 3(2021) Page Start: 534 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Update of spectrum c.35delG and c.‐23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss. (3rd September 2018) Authors: Azadegan‐Dehkordi, Fatemeh; Ahmadi, Reza; Koohiyan, Mahbobeh; Hashemzadeh‐Chaleshtori, Morteza Journal: Annals of human genetics Issue: Volume 83:Number 1(2019:Jan.) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗