Hasil Pencarian - Mohammad Farid Mohammadi

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  1. 1
    Whole‐exome sequencing identified first homozygous frameshift variant in the COLEC10 gene in an Iranian patient causing 3MC syndrome type 3

    Whole‐exome sequencing identified first homozygous frameshift variant in the COLEC10 gene in an Iranian patient causing 3MC syndrome type 3 oleh Pouria Mohammadi, Elham Salehi Siavashani, Mohammad Farid Mohammadi, Afshin Bahramy, Navid Almadani, Masoud Garshasbi

    Diterbitkan 2021-11-01
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  2. 2
    Expression assay of the COLQ in a family with congenital myasthenic syndrome and symptomatic carriers

    Expression assay of the COLQ in a family with congenital myasthenic syndrome and symptomatic carriers oleh Mohammad Farid Mohammadi, Sahand Tehrani Fateh, Hadi Aghajani, Afshin Bahramy, Seyed Mohammad Salar Zaheryani, Javad Behroozi, Seyyed Mohammad Kahani, Pouria Mohammadi, Masoud Garshasbi

    Diterbitkan 2023-10-01
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