Showing 1 - 3 results of 3 for search 'Sima Rayat', query time: 0.04s Refine Results
  1. 1
    Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness

    Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness by Sima Rayat, Mohammad Farhadi, Hessamaldin Emamdjomeh, Saeid Morovvati, Masoumeh Falah

    Published 2022
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  2. 2
    Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation

    Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation by Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Mohammad Keramatipour, Saeid Morovvati

    Published 2021
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  3. 3
    Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report

    Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report by Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Aliagha Alishiri, Mohammad Keramatipour, Zeynab Javanfekr Shahri, Saeid Morovvati

    Published 2021
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