Search Results - Noushin Nik-Zaat

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    Linkage Analysis for 50 Iranian Families with Autosomal Recessive Non-Syndromic Hearing Loss for DFNB21 Locus by Parisa Imani-Raad, Kimia Kahrizi, Niloufar Bazzaz-Zadegan, Marzieh Mohseni, Golnaz As'adi, Noushin Nik-Zaat, Fatemeh Sadat Esteghamat, Hossein Najm-Abadi

    Published 2006
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    Prevalence Study of GJB2 Gene Mutations in Iranian Ethnics by Kimia Kahrizi, Niloufar Bazzaz-Zadegan, Marzieh Mohseni, Noushin Nik-Zaat, Khadijeh Jalalvand, Yaser Riaz-el Hosseini, Yousef Shafeghati, Sanaz Arzhangi, Khalil Javan, Hosein Najmabadi

    Published 2007
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