Items where Author is "Sanati, Mohammad Hossein."

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 7.

Article

Reiisi, Somayeh. and Tabatabaiefar, Mohammad Amin. and Sanati, Mohammad Hossein. and Hashemzadeh-Chaleshtori, Morteza. (2016) Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family. Iranian Journal of Basic Medical Sciences, 19 (7). pp. 772-778.

Reiisi, Somayeh. and Sanati, Mohammad Hossein. and Tabatabaiefar, Mohammad Amin. and Ahmadian, Shahla. and Reiisi, Salimeh. and Parchami Barjui, Shahrbanoo. and Porjafari, Hamid. and Shahi, Heshmat. and Shavarzi, Afsaneh. and Hashemzadeh-Chaleshtori, Morteza. (2014) The Study of SLC26A4 Gene Causing Autosomal Recessive Hearing Loss by Linkage Analysis in a Cohort of Iranian Populations. International journal of molecular and cellular medicine, 3 (3). pp. 176-82. ISSN 2251-9637

Reiisi, Somayeh. and Sanati, Mohammad Hossein. and Tabatabaiefar, Mohammad Amin. and PourJafari, Hamid Reza. and Minuchehr, Zarrin. and Shavarzi, Afsaneh. and Ataiee, Mitra. and kasiri, mahboobeh. and Hashemzadeh-Chaleshtori, Morteza. (2014) Study of the association of DFNB3 locus with autosomal recessive non-syndromic hearing loss in iranian deaf population using genetic linkage analysis. Journal of Isfahan Medical School, 32 (285). pp. 669-677.

Sadeghi, Abdolrahim. and Sanati, Mohammad Hossein. and Alasti, Fatemeh. and Hashemzadeh-Chaleshtori, Morteza. and Mahmoudian, Saeid. and Ataei, Mitra. (2009) Contribution of GJB2 mutations and Four common DFNB loci in autosomal recessive non-syndromic hearing impairment in Markazi and Qom provinces of Iran. Iranian Journal of Biotechnology, 7 (2). 108-111+120.

Banoei, Mohammad Mehdi. and Hashemzadeh-Chaleshtori, Morteza. and Sanati, Mohammad Hossein. and Shariati, PARVIN. and Houshmand, MASSOUD. and Majidizadeh, TAYEBEH. and Jahangir Soltani, NILOOFAR. and Golalipour, MASSOUD. (2008) Variation of DAT1 VNTR alleles and genotypes among old ethnic groups in Mesopotamia to the Oxus region. Human Biology, 80 (1). pp. 73-81.

Banoei, Mohammad Mehdi. and Hashemzadeh-Chaleshtori, Morteza. and Sanati, Mohammad Hossein. and Shafa Sharait Panahi, Mehdi. and Majidizadeh, TAYEBEH. and Rostami, Maryam. and DEHGHAN Manshadi, Massoumeh. and Golalipour, Masoud. (2007) Diversity and relationship between Iranian ethnic groups: Human dopamine transporter gene (DAT1) VNTR genotyping. American Journal of Human Biology, 19 (6). pp. 821-826.

Sadeghi, Abdolrahim. and Sanati, Mohammad Hossein. and Alasti, Fatemeh. and Ataei, Mitra. and Hashemzadeh-Chaleshtori, Morteza. (2005) Mutation analysis of connexin 26 gene and del (GJB6-D13S1830) in patients with hereditary deafness from two provinces in Iran. IRANIAN JOURNAL OF BIOTECHNOLOGY, 3 (4).

This list was generated on Thu Apr 2 01:12:10 2020 IRDT.