Items where Author is "Abdollahi, S."

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Jamshidi, J. and Abdollahi, S. and Ghaedi, H. and Alehabib, E. and Tafakhori, A. and Alinaghi, S. and Chapi, M. and Johari, A.H. and Darvish, H. (2017) A novel mutation in SMOC1 and variable phenotypic expression in two patients with Waardenburg anophthalmia syndrome. European Journal of Medical Genetics.

Shahmohammadibeni, N. and Rahimi-Aliabadi, S. and Jamshidi, J. and Emamalizadeh, B. and Shahmohammadibeni, H.A. and Zare Bidoki, A. and Akhavan-Niaki, H. and Eftekhari, H. and Abdollahi, S. and Shekari Khaniani, M. and Shahmohammadibeni, M. and Fazeli, A. and Motallebi, M. and Taghavi, S. and Ahmadifard, A. and Shafiei Zarneh, A.E. and Andarva, M. and Dadkhah, T. and Khademi, E. and Alehabib, E. and Rahimi, M. and Tafakhori, A. and Atakhorrami, M. and Darvish, H. (2016) The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson�s disease in Iranian population. Neurological Sciences, 37 (5). pp. 731-736.

Haghnejad, L. and Emamalizadeh, B. and Jamshidi, J. and Bidoki, A.Z. and Ghaedi, H. and Ahmadi, E. and Abdollahi, S. and Shahmohammadibeni, N. and Taghavi, S. and Fazeli, A. and Motallebi, M. and Zarneh, A.E.S. and Mohammadihosseinabad, S. and Abbaszadegan, M.R. and Torkamandi, S. and Gavenaroudi, M.A. and Pedram, N. and Shahidi, G.-A. and Tafakhori, A. and Darvish, H. and Movafagh, A. (2015) Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian population. Journal of the Neurological Sciences, 355 (1-2). pp. 72-74.

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