Showing 1 - 3 results of 3 for search 'Marjan MASOUDI', query time: 0.02s Refine Results
  1. 1
    Investigating the relationship of genetic mutations in GJB2 and linkage analysis of DFNB4 Locus in a group of non-syndromic hearing impaired people with autosomal recessive inheritance in Hormozgan

    Investigating the relationship of genetic mutations in GJB2 and linkage analysis of DFNB4 Locus in a group of non-syndromic hearing impaired people with autosomal recessive inherit... by Najmeh Ahangari, Marjan Masoudi, Aliakbar Poursadegh, Abdolazim Nejatizadeh

    Published 2014-12-01
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    Article
  2. 2
    Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss

    Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss by Marjan MASOUDI, Najmeh AHANGARI, Ali Akbar POURSADEGH ZONOUZI, Ahmad POURSADEGH ZONOUZI, Azim NEJATIZADEH

    Published 2016-05-01
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  3. 3
    Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran

    Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndrom... by Masoud Akbarzadeh Laleh, Marzieh Naseri, Ali Akbar Poursadegh Zonouzi, Ahmad Poursadegh Zonouzi, Marjan Masoudi, Najmeh Ahangari, Leila Shams, Azim Nejatizadeh

    Published 2017-01-01
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    Article

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