Search Results - Farshid Parvini

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  1. 1
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    A novel de novo nonsense mutation in SALL4 causing duane radial ray syndrome: a case report and expanding the phenotypic spectrum by Mobarakeh Ajam-Hosseini, Farshid Parvini, Abdolhamid Angaji

    Published 2023
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  2. 2
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    A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss by Hossein Fahimi, Samira Behroozi, Sadaf Noavar, Farshid Parvini

    Published 2021
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    Association of IL-10 gene promoter polymorphisms with susceptibility to pseudoexfoliation syndrome, pseudoexfoliative and primary open-angle glaucoma by Ghasem Fakhraie, Farshid Parvini, Jalaledin Ghanavi, Shima Saif, Poopak Farnia

    Published 2020
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    A novel homozygous frame-shift mutation in the SLC29A3 gene: a new case report and review of literature by Sadaf Noavar, Samira Behroozi, Taraneh Tatarcheh, Farshid Parvini, Majid Foroutan, Hossein Fahimi

    Published 2019
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