Torthaí cuardaigh - Daneshjoo, Omid

  • 1 - 3 toradh as 3 á dtaispeáint
Beachtaigh na torthaí
  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 de réir Daneshjoo, Omid, Garshasbi, Masoud

    Foilsithe / Cruthaithe 2018
    Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán
    Téacs
    Cuir le mo chuid Ceanán
    Sábháilte in:
  2. 2
    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 de réir Daneshjoo, Omid, Salehi, Leila B., Pizzuti, Antonio, Novelli, Giuseppe, Sangiuolo, Federica

    Foilsithe / Cruthaithe 2020
    Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán
    Téacs
    Cuir le mo chuid Ceanán
    Sábháilte in:
  3. 3
    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 de réir Daneshjoo, Omid, Ebrahimi, Pirooz, Salehi, Leila B., Pizzuti, Antonio, Garshasbi, Masoud

    Foilsithe / Cruthaithe 2020
    Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán
    Téacs
    Cuir le mo chuid Ceanán
    Sábháilte in:

Uirlisí cuardaigh: