Showing 1 - 12 results of 12 for search 'M Montazer zohour', query time: 0.08s Refine Results
  1. 1
    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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  2. 2
    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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  3. 3
    Report of a New Mutation and Frequency of Connexin 26 gene (GJB2) Mutations in Patients from Three Provinces of Iran

    Report of a New Mutation and Frequency of Connexin 26 gene (GJB2) Mutations in Patients from Three Provinces of Iran by A Hosseinipour, M Hashemzadeh Chaleshtori, R Sasanfar, DD Farhud, A Tolooi, M Doulati, L Hoghooghi Rad, M Montazer zohour, M Ghadami

    Published 2005
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  4. 4
    Report of a New Mutation and Frequency of Connexin 26 gene (GJB2) Mutations in Patients from Three Provinces of Iran

    Report of a New Mutation and Frequency of Connexin 26 gene (GJB2) Mutations in Patients from Three Provinces of Iran by A Hosseinipour, M Hashemzadeh Chaleshtori, R Sasanfar, DD Farhud, A Tolooi, M Doulati, L Hoghooghi Rad, M Montazer zohour, M Ghadami

    Published 2005
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  5. 5
    "Frequency of A Very Rare 35delG Mutation in Two Ethnic Groups of Iranian Populations "

    "Frequency of A Very Rare 35delG Mutation in Two Ethnic Groups of Iranian Populations " by R Sasanfar, A Tolouei, A Hoseinipour, DD Farhud, M Dolati, L Hoghooghi Rad, M Montazer Zohour, M Ghadami, H Pour-Jafari, M Hashemzadeh Chaleshtori

    Published 2004
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  6. 6
    "Frequency of A Very Rare 35delG Mutation in Two Ethnic Groups of Iranian Populations "

    "Frequency of A Very Rare 35delG Mutation in Two Ethnic Groups of Iranian Populations " by R Sasanfar, A Tolouei, A Hoseinipour, DD Farhud, M Dolati, L Hoghooghi Rad, M Montazer Zohour, M Ghadami, H Pour-Jafari, M Hashemzadeh Chaleshtori

    Published 2004
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  7. 7
    Frequencies of Mutations in the Connexin 26 Gene (GJB2) in Two Populations of Iran (Tehran and Tabriz)

    Frequencies of Mutations in the Connexin 26 Gene (GJB2) in Two Populations of Iran (Tehran and Tabriz) by M Hashemzadeh Chaleshtori, L Hoghooghi Rad, M Dolati, R Sasanfar, A Hoseinipour, M Montazer Zohour, H Pourjafari, A Tolooi, M Ghadami, DD Farhud, MA Patton

    Published 2005
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  8. 8
    Frequencies of Mutations in the Connexin 26 Gene (GJB2) in Two Populations of Iran (Tehran and Tabriz)

    Frequencies of Mutations in the Connexin 26 Gene (GJB2) in Two Populations of Iran (Tehran and Tabriz) by M Hashemzadeh Chaleshtori, L Hoghooghi Rad, M Dolati, R Sasanfar, A Hoseinipour, M Montazer Zohour, H Pourjafari, A Tolooi, M Ghadami, DD Farhud, MA Patton

    Published 2005
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  9. 9
    "Two Novel Mutations and Predominant 35delG Mutation in the Connexin 26 Gene (GJB2) in Iranian Populations"

    "Two Novel Mutations and Predominant 35delG Mutation in the Connexin 26 Gene (GJB2) in Iranian Populations" by "M Hashemzadeh Chaleshtori, M Dowlati, DD Farhud, L Hoghooghi Rad, R Sasanfar A Hoseinipour, M Montazer Zohour, A Tolooi, M Ghadami, HR Pourjafari, MA Oshaghi, MA Patton "

    Published 2004
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  10. 10
    "Two Novel Mutations and Predominant 35delG Mutation in the Connexin 26 Gene (GJB2) in Iranian Populations"

    "Two Novel Mutations and Predominant 35delG Mutation in the Connexin 26 Gene (GJB2) in Iranian Populations" by "M Hashemzadeh Chaleshtori, M Dowlati, DD Farhud, L Hoghooghi Rad, R Sasanfar A Hoseinipour, M Montazer Zohour, A Tolooi, M Ghadami, HR Pourjafari, MA Oshaghi, MA Patton "

    Published 2004
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  11. 11
    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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  12. 12
    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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