Showing 1 - 3 results of 3 for search 'Akram Sarmadi', query time: 0.01s Refine Results
  1. 1
    Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia

    Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsi... by Zahra Nouri, Akram Sarmadi, Sina Narrei, Hamidreza Kianersi, Farzan Kianersi, Mohammad Amin Tabatabaiefar

    Published 2024-07-01
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  2. 2
    Correction: Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia

    Correction: Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and... by Zahra Nouri, Akram Sarmadi, Sina Narrei, Hamidreza Kianersi, Farzan Kianersi, Mohammad Amin Tabatabaiefar

    Published 2025-08-01
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  3. 3
    A novel NBN germline mutation as the likely inherited etiology of various cancer types in an Iranian family

    A novel NBN germline mutation as the likely inherited etiology of various cancer types in an Iranian family by Akram Sarmadi, Samaneh Adelian, Zahra Nouri, Shaghayegh Haghjooy Javanmard, Rasoul Omidzadeh, Mohammad Amin Tabatabaiefar

    Published 2025-05-01
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