Hasil Pencarian - Farshid Parvini

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  1. 1
    A novel de novo nonsense mutation in SALL4 causing duane radial ray syndrome: a case report and expanding the phenotypic spectrum

    A novel de novo nonsense mutation in SALL4 causing duane radial ray syndrome: a case report and expanding the phenotypic spectrum oleh Mobarakeh Ajam-Hosseini, Farshid Parvini, Abdolhamid Angaji

    Diterbitkan 2023-02-01
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  2. 2
    A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss

    A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss oleh Hossein Fahimi, Samira Behroozi, Sadaf Noavar, Farshid Parvini

    Diterbitkan 2021-02-01
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  3. 3
    Gram-negative bacterial sRNAs encapsulated in OMVs: an emerging class of therapeutic targets in diseases

    Gram-negative bacterial sRNAs encapsulated in OMVs: an emerging class of therapeutic targets in diseases oleh Mobarakeh Ajam-Hosseini, Fatemeh Akhoondi, Farshid Parvini, Hossein Fahimi

    Diterbitkan 2024-01-01
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  4. 4
    Association of IL-10 gene promoter polymorphisms with susceptibility to pseudoexfoliation syndrome, pseudoexfoliative and primary open-angle glaucoma

    Association of IL-10 gene promoter polymorphisms with susceptibility to pseudoexfoliation syndrome, pseudoexfoliative and primary open-angle glaucoma oleh Ghasem Fakhraie, Farshid Parvini, Jalaledin Ghanavi, Shima Saif, Poopak Farnia

    Diterbitkan 2020-02-01
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  5. 5
    A novel homozygous frame-shift mutation in the SLC29A3 gene: a new case report and review of literature

    A novel homozygous frame-shift mutation in the SLC29A3 gene: a new case report and review of literature oleh Sadaf Noavar, Samira Behroozi, Taraneh Tatarcheh, Farshid Parvini, Majid Foroutan, Hossein Fahimi

    Diterbitkan 2019-08-01
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