Showing 1 - 4 results of 4 for search 'K Safa Chaleshtori', query time: 0.03s Refine Results
  1. 1
    Molecular Pathology of 6 Novel GJB2 Allelic Variants Detected in Familial and Sporadic Iranian Non Syndromic Hearing Loss Cases

    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 2008
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  2. 2
    Molecular Pathology of 6 Novel GJB2 Allelic Variants Detected in Familial and Sporadic Iranian Non Syndromic Hearing Loss Cases

    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 2008
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  3. 3
    Autosomal Recessive and Sporadic Non Syndromic Hearing Loss and the Incidence of Cx26 Mutations in a Province of Iran

    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 2006
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  4. 4
    Autosomal Recessive and Sporadic Non Syndromic Hearing Loss and the Incidence of Cx26 Mutations in a Province of Iran

    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 2006
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