Elham Ehsani

Phenotype of ST3GAL3 Deficient Patients: a Case and Review of the Literature.

M. Dianatpour, Marjan Masoudi, S. Mohammadi, 2021, European journal of medical genetics.

MCM2 mutation causes autosomal dominant nonsyndromic hearing loss (DFNA70): novel variant in the second family

M. Dianatpour, S. Mohammadi, Zahra Zeraatpisheh, 2022, Journal of genetics.

MCM2 mutation causes autosomal dominant nonsyndromic hearing loss (DFNA70): novel variant in the second family

M. Dianatpour, S. Mohammadi, Zahra Zeraatpisheh, 2022, Journal of Genetics.