Items where Author is "Rashki, Ahmad."

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Article

Moradipour, Negar. and Ghasemi-Dehkordi, Payam. and Heibati, Fatemeh. and Parchami Barjui, Shahrbanoo. and Abolhasani, Marziyeh. and Rashki, Ahmad. and Hashemzadeh-Chaleshtori, Morteza. (2016) Mutation screening of exons 7 and 13 of the TMC1 gene in autosomal recessive non-syndromic hearing loss (ARNSHL) in Iran. Iranian Red Crescent Medical Journal, 18 (2).

Azadegan-Dehkordi, Fatemeh. and Rashki, Ahmad. and Bagheri, Nader. and Hashemzadeh-Chaleshtori, Morteza. and Memarzadeh, Ezzatollah. and Salehi, Ali. and Ghatreh, Homan. and Zandi, Farid. and Yazdanpanahi, Nasrin. and Tabatabaiefar, Mohammad Amin. and Hashemzadeh-Chaleshtori, Morteza. (2013) Study of VSX1 Mutations in Patients with Keratoconus in Southwest Iran Using PCR-Single-Strand Conformation Polymorphism/Heteroduplex Analysis and Sequencing Method. ACTA CYTOLOGICA, 57 (6). pp. 646-651.

Azadegan-Dehkordi, Fatemeh. and Rashki, Ahmad. and Bagheri, Nader. and Hashemzadeh-Chaleshtori, Minoo. and Memarzadeh, Ezzatollah. and Salehi, Ali. and Ghatreh, Homan. and Hydari, Soraya. and Yazdanpanahi, Nasrin. and Rashki Ghalehnoo, Zahra. and Merzaeyan, Amin. and Hashemzadeh-Ghalehstori, Morteza. (2013) Studying VSX1 gene mutations in patients with Keratoconus of Chaharmahal and Bakhtiari province, Iran. Journal of Kerman University of Medical Sciences, 20 (6). pp. 546-554.

This list was generated on Thu Jun 27 01:08:43 2019 IRDT.