Showing 1 - 20 results of 21 for search 'H. Pour Jafari', query time: 0.12s
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Molecular Pathology of 6 Novel GJB2 Allelic Variants Detected in Familial and Sporadic Iranian Non Syndromic Hearing Loss Cases by M Hashemzadeh Chaleshtori, DD Farhud, AH Crosby, E Farrokhi, H Pour Jafari, K Ghatreh Samani, K Safa Chaleshtori, M Kasiri, M Shahrani, GR Mobini, M Mansouri, D Modarresinia, M Jafari
Published 2008Connect to this object online.
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19
Molecular Pathology of 6 Novel GJB2 Allelic Variants Detected in Familial and Sporadic Iranian Non Syndromic Hearing Loss Cases by M Hashemzadeh Chaleshtori, DD Farhud, AH Crosby, E Farrokhi, H Pour Jafari, K Ghatreh Samani, K Safa Chaleshtori, M Kasiri, M Shahrani, GR Mobini, M Mansouri, D Modarresinia, M Jafari
Published 2008Connect to this object online.
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20
Autosomal Recessive and Sporadic Non Syndromic Hearing Loss and the Incidence of Cx26 Mutations in a Province of Iran by M Hashemzadeh Chaleshtori, M Montazer Zohour, L Hoghooghi Rad, H Pour-Jafari, DD Farhud, M Dolati, K Safa Chaleshtori, R Sasanfar, A Hosseinipour, L Andonian, A Tolouei, M Ghadami, MA Patton
Published 2006Connect to this object online.
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