Resultados de búsqueda - Daneshjoo, Omid

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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 por Daneshjoo, Omid, Garshasbi, Masoud

    Publicado 2018
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    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 por Daneshjoo, Omid, Salehi, Leila B., Pizzuti, Antonio, Novelli, Giuseppe, Sangiuolo, Federica

    Publicado 2020
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    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 por Daneshjoo, Omid, Ebrahimi, Pirooz, Salehi, Leila B., Pizzuti, Antonio, Garshasbi, Masoud

    Publicado 2020
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