Items where Author is "Bonyadi, Mortaza"

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Mehdizadeh Fanid, Leila and Shahrokhi, Hassan and Adampourezare, Mina and Hosseinpour Feizi, Mohamad Ali and Bonyadi, Mortaza and Eslami, A (2015) Association between Common Single- nucleotide Polymorphism of Reelin Gene, rs736707 (C/T) with Autism Spectrum Disorder in Iranian-Azeri Patients. International Journal of Pediatrics, 3 (6.1). pp. 1065-1071.

Bonyadi, Mortaza and Ranjbar Rad, Sanaz and Jabbarpour Bonyadi, Mohammad Hossein and Ahmadieh, Hamid (2015) Association of C3 gene polymorphism with age related macular degeneration in Gonabad region from NorthEast of Iran. medical journal of mashhad university of medical sciences, 58 (3). pp. 156-161.

This list was generated on Sat Jul 11 11:25:32 2020 EDT.