Items where Author is "Ahmadieh, H."

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Article

Safarpour Lima, B. and Ghaedi, H. and Daftarian, N. and Ahmadieh, H. and Jamshidi, J. and Khorrami, M. and Noroozi, R. and Sohrabifar, N. and Assarzadegan, F. and Hesami, O. and Taghavi, S. and Ahmadifard, A. and Atakhorrami, M. and Rahimi-Aliabadi, S. and Shahmohammadibeni, N. and Alehabib, E. and Andarva, M. and Darvish, H. and Emamalizadeh, B. (2016) C.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness. European Journal of Medical Genetics, 59 (2). pp. 65-69.

Rahimi-Aliabadi, S. and Daftarian, N. and Ahmadieh, H. and Emamalizadeh, B. and Jamshidi, J. and Tafakhori, A. and Ghaedi, H. and Noroozi, R. and Taghavi, S. and Ahmadifard, A. and Alehabib, E. and Andarva, M. and Shokraeian, P. and Atakhorrami, M. and Darvish, H. (2016) A novel mutation and variable phenotypic expression in a large consanguineous pedigree with Jalili syndrome. Eye (Basingstoke), 30 (11). pp. 1424-1432.

This list was generated on Tue Oct 20 04:57:37 2020 EDT.