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  1. 1
    Frequency of GJB2 mutations, GJB6‐D13S1830 and GJB6‐D13S1854 deletions among patients with non‐syndromic hearing loss from the central region of Iran

    Frequency of GJB2 mutations, GJB6‐D13S1830 and GJB6‐D13S1854 deletions among patients with non‐syndromic hearing loss from the central region of Iran von Naddafnia, Hossein, Noormohammadi, Zahra, Irani, Shiva, Salahshoorifar, Iman


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  2. 2
    Association between IL-6 -174 G/C (rs1800795) and IL-1A -889 C/T (rs1800587) cytokine variants with polycystic ovary syndrome in Iranian women: A case-control study

    Association between IL-6 -174 G/C (rs1800795) and IL-1A -889 C/T (rs1800587) cytokine variants with polycystic ovary syndrome in Iranian women: A case-control study von Farhad Sadr Tabatabaie, Seyed, Salahshoorifar, Iman, Pouresmaeili, Farkhondeh, Hosseinpour Golloo, Zahra, aarabi, Azadeh, Kholghi Oskooei, Vahid, Vatannejad, Akram

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  3. 3
    Whole Exome Sequencing of Non-Syndromic Hearing Loss Patients

    Whole Exome Sequencing of Non-Syndromic Hearing Loss Patients von Naddafnia, Hossein, Noormohammadi, Zahra, Irani, Shiva, Salahshoorifar, Iman


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  4. 4
    Frequency of GJB 2 mutations, GJB 6‐D13S1830 and GJB 6‐D13S1854 deletions among patients with non‐syndromic hearing loss from the central region of Iran

    Frequency of GJB 2 mutations, GJB 6‐D13S1830 and GJB 6‐D13S1854 deletions among patients with non‐syndromic hearing loss from the central region of Iran von Naddafnia, Hossein, Noormohammadi, Zahra, Irani, Shiva, Salahshoorifar, Iman


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