Items where Author is "NAJMABADI, Hossein"

Article

AKBARIAZAR, Elinaz and Reza EBRAHIMPOUR, Mohammad and AKBARI, Saeedeh and ARZHANGHI, Sanaz and Sedigheh ABEDINI, Seydeh and NAJMABADI, Hossein and KAHRIZI, Kimia (2013) A novel deletion mutation in ASPM gene in an Iranian family with autosomal recessive primary microcephaly. Iranian Journal of Child Neurology, 7 (2). pp. 23-30.