The Study of SLC26A4 Gene Causing Autosomal Recessive Hearing Loss by Linkage Analysis in a Cohort of Iranian Populations von Reiisi, Somayeh, Sanati, Mohammad Hosein, Tabatabaiefar, Mohammad Amin, Ahmadian, Shahla, Reiisi, Salimeh, Parchami, Shahrbanoo, Porjafari, Hamid, Shahi, Heshmat, Shavarzi, Afsaneh, Hashemzade Chaleshtori, Morteza

Volltext

FISH analysis for del6q21 and del17p13 in b-cell chronic lymphocytic leukemia in Iranians von Ashuri, Saidi, Taymuri, Husayn, Akbari, Muhammad Taghi, Chaleshtori, Murtada Hashim Zadah, Naeini, Marjan Mojtabavi

Volltext

A novel TECTA mutation causes autosomal recessive non-syndromic hearing loss in Iranian kindred von Asgharzade, Samira, Tabatabaiefar, Mohammad Amin, Modarressi, Mohammad Hossein, Ghahremani, Mohammad Hossein, Reiisi, Somayeh, Tahmasebi, Parisa, Abdollahnejad, Fatemeh, Chaleshtori, Morteza Hashemzade

Volltext

Mutation in second exon of MYO15A gene cause of nonsyndromic hearing loss and its association in the Arab population in Iran von Asgharzade, Samira, Chaleshtori, Morteza, Tabatabaifar, Mohammad, Reisi, Somayeh, Modaressi, Mohammad

Volltext