Items where Author is "Arabi, A."

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Rafigh, M. and Salmaninejad, A. and Sorouri Khorashad, B. and Arabi, A. and Milanizadeh, S. and Hiradfar, M. and Abbaszadegan, M. R. (2020) Novel Deleterious Mutation in Steroid-5α-Reductase-2 in 46, XY Disorders of Sex Development: Case Report Study. Fetal and Pediatric Pathology.

Ghaemi, H. and Sobhani-Rad, D. and Arabi, A. and Saifpanahi, S. and Anaraki, Z. G. (2016) Review paper: Role of basal ganglia in swallowing process. Iranian Rehabilitation Journal, 14 (4). pp. 239-245.

Moghbeli, M. and Maleknejad, M. and Arabi, A. and Abbaszadegan, M. R. (2012) Mutational analysis of uroporphyrinogen III cosynthase gene in Iranian families with congenital erythropoietic porphyria. Molecular Biology Reports, 39 (6). pp. 6731-6735.

This list was generated on Sun Apr 18 22:26:48 2021 EDT.