New distribution record of Phrynocephalus mystaceus Pallas 1776 (Sauria: Agamidae) from Iran von Molavi, Farahnaz, Mohammadian-kalat, Tooba, Kiabi, Bahram Hasanzade, Kami, Haji Gholi, Yazdanpanahi, Morteza

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Karyological study of the Caspian bent-toed Gecko Cyrtopodion caspium (Sauria: Gekkonidae) from North and North-Eastern of Iran von Faranaz Molavi, Haji GholiKami, Morteza Yazdanpanahi

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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 von Azadegan-Dehkordi, Fatemeh, Bahrami, Tayyebe, Shirzad, Maryam, Karbasi, Gelareh, Yazdanpanahi, Nasrin, Farrokhi, Effat, Koohiyan, Mahbobeh, Tabatabaiefar, Mohammad Amin, Hashemzadeh-Chaleshtori, Morteza

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A novel variant of SLC26A4 and first report of the c.716T>A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss von Azadegan-Dehkordi, Fatemeh, Ahmadi, Reza, Bahrami, Tayyeb, Yazdanpanahi, Nasrin, Farrokhi, Effat, Tabatabaiefar, Mohammad Amin, Hashemzadeh-Chaleshtori, Morteza

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Detection of two pathogenesis previously unreported myosin xva pathogenic variants in two large Iranian pedigrees with autosomal recessive nonsyndromic hearing loss von Azadegan-Dehkordi, Fatemeh, Ashrafi, Korosh, Mobini, Gholam, Yazdanpanahi, Nasrin, Shirzad, Maryam, Farrokhi, Effat, Hashemzadeh-Chaleshtori, Morteza

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Compound Heterozygosity for Two Novel SLC26A4 Mutations in a Large Iranian Pedigree with Pendred Syndrome von Yazdanpanahi, Nasrin, Tabatabaiefar, Mohammad Amin, Farrokhi, Effat, Abdian, Narges, Bagheri, Nader, Shahbazi, Shirin, Noormohammadi, Zahra, Chaleshtori, Morteza Hashemzadeh

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Mutation analysis of GJB2 and GJB6 genes and screening of nine common dfnb loci in iranian pedigrees with autosomal recessive nonsyndromic hearing loss von Azadegan-Dehkordi, Fatemeh, Koohiyan, Mahbobeh, Shirzad, Maryam, Bahrami, Tayyeb, Yazdanpanahi, Nasrin, Tabatabaiefar, Mohammad, Pourpaknia, Reza, Farrokhi, Effat, Hashemzadeh-Chaleshtori, Morteza

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Study of VSX1 Mutations in Patients with Keratoconus in Southwest Iran Using PCR-Single-Strand Conformation Polymorphism/Heteroduplex Analysis and Sequencing Method von Dehkordi, Fatemeh Azadegan, Rashki, Ahmad, Bagheri, Nader, Chaleshtori, Minoo Hashemzadeh, Memarzadeh, Ezzatollah, Salehi, Ali, Ghatreh, Homan, Zandi, Farid, Yazdanpanahi, Nasrin, Tabatabaiefar, Mohammad Amin, Chaleshtori, Morteza Hashemzadeh

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Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss von Yazdanpanahi, Nasrin, Chaleshtori, Morteza Hashemzadeh, Tabatabaiefar, Mohammad Amin, Noormohammadi, Zahra, Farrokhi, Effat, Najmabadi, Hossein, Shahbazi, Shirin, Hosseinipour, Azam

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Investigation of LRTOMT gene (locus DFNB63) mutations in Iranian patients with autosomal recessive non-syndromic hearing loss von Taghizadeh, Seyyed Hossein, Kazeminezhad, Seyyed Reza, Sefidgar, Seyyed Ali Asghar, Yazdanpanahi, Nasrin, Tabatabaeifar, Mohammad Amin, Yousefi, Ahmad, Lesani, Seyyed Mohammad, Abolhasani, Marziyeh, Hashemzadeh Chaleshtori, Morteza

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Compound Heterozygosity for Two Novel Mutations in a Large Iranian Pedigree with Pendred Syndrome von Nasrin Yazdanpanahi, Mohammad Amin Tabatabaiefar, Effat Farrokhi, Narges Abdian, Nader Bagheri, Shirin Shahbazi, Zahra Noormohammadi, Morteza Hashemzadeh Chaleshtori

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