Hakutulokset - Daneshjoo, Omid

  • Näytetään 1 - 3 yhteensä 3 tuloksesta
Tarkenna hakua
  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 Tekijä Daneshjoo, Omid, Garshasbi, Masoud

    Julkaistu 2018
    Hae kokoteksti Hae kokoteksti Hae kokoteksti
    Teksti
    Lisää suosikkeihin
    Tallennettuna:
  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 Tekijä Daneshjoo, Omid, Salehi, Leila B., Pizzuti, Antonio, Novelli, Giuseppe, Sangiuolo, Federica

    Julkaistu 2020
    Hae kokoteksti Hae kokoteksti Hae kokoteksti
    Teksti
    Lisää suosikkeihin
    Tallennettuna:
  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 Tekijä Daneshjoo, Omid, Ebrahimi, Pirooz, Salehi, Leila B., Pizzuti, Antonio, Garshasbi, Masoud

    Julkaistu 2020
    Hae kokoteksti Hae kokoteksti Hae kokoteksti
    Teksti
    Lisää suosikkeihin
    Tallennettuna:

Työkalut: