Hasil Pencarian - Omid Daneshjoo

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  1. 1
    Novel compound heterozygote mutations in the ATP7B gene in an Iranian family with Wilson disease: a case report

    Novel compound heterozygote mutations in the ATP7B gene in an Iranian family with Wilson disease: a case report oleh Omid Daneshjoo, Masoud Garshasbi

    Diterbitkan 2018-03-01
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  2. 2
    Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family

    Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family oleh Omid Daneshjoo, Pirooz Ebrahimi, Leila B. Salehi, Antonio Pizzuti, Masoud Garshasbi

    Diterbitkan 2020-12-01
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  3. 3
    An enormous Italian pedigree of Marfan syndrome with a novel mutation in the FBN1 gene

    An enormous Italian pedigree of Marfan syndrome with a novel mutation in the FBN1 gene oleh Omid Daneshjoo, Leila B. Salehi, Antonio Pizzuti, Giuseppe Novelli, Federica Sangiuolo

    Diterbitkan 2020-08-01
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