Omid Daneshjoo
2PUBLICATIONS
3CO-AUTHORS
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Publications (2)
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|Dec 28, 2020
Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family.Omid Daneshjoo, Pirooz Ebrahimi, Leila B Salehi
|Sep 05, 2020
An enormous Italian pedigree of Marfan syndrome with a novel mutation in the FBN1 gene.Omid Daneshjoo, Leila B Salehi, Antonio Pizzuti
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