Showing 1 - 6 results of 6 for search 'E Farrokhi', query time: 0.03s Refine Results
  1. 1
    The -514C/T Polymorphism of Hepatic Lipase Gene among Iranian Patients with Coronary Heart Disease

    The -514C/T Polymorphism of Hepatic Lipase Gene among Iranian Patients with Coronary Heart Disease by K Ghatreh Samani, M Noori, M Rohbani Nobar, M Hashemzadeh Chaleshtory, E Farrokhi, M Darabi Amin

    Published 2012
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  2. 2
    The -514C/T Polymorphism of Hepatic Lipase Gene Among Iranian Patients with Coronary Heart Disease

    The -514C/T Polymorphism of Hepatic Lipase Gene Among Iranian Patients with Coronary Heart Disease by M Darabi Amin, E Farrokhi, M Hashemzadeh Chaleshtory, M Rohbani Nobar, M Noori, K Ghatreh Samani

    Published 2012
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  3. 3
    Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss

    Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss by MA Tabatabaiefar, F Alasti, M Montazer Zohour, L Shariati, E Farrokhi, DD Farhud, GV Camp, MR Noori-Daloii, M Hashemzadeh Chaleshtori

    Published 2011
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  4. 4
    Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss

    Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss by MA Tabatabaiefar, F Alasti, M Montazer Zohour, L Shariati, E Farrokhi, DD Farhud, GV Camp, MR Noori-Daloii, M Hashemzadeh Chaleshtori

    Published 2011
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  5. 5
    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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  6. 6
    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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