Items where Author is "Pouriran, R."

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Article

Andarva, M. and Jamshidi, J. and Ghaedi, H. and Daftarian, N. and Emamalizadeh, B. and Alehabib, E. and Taghavi, S. and Pouriran, R. and Darvish, H. (2018) A novel c.240241insGG mutation in NDP gene in a family with Norrie disease. Clinical and Experimental Optometry.

Andarva, M. and Jamshidi, J. and Ghaedi, H. and Daftarian, N. and Emamalizadeh, B. and Alehabib, E. and Taghavi, S. and Pouriran, R. and Darvish, H. (2018) A novel c.240241insGG mutation in NDP gene in a family with Norrie disease. Clinical and Experimental Optometry, 101 (2). pp. 255-259.

Khademi, E. and Alehabib, E. and Shandiz, E.E. and Ahmadifard, A. and Andarva, M. and Jamshidi, J. and Rahimi-Aliabadi, S. and Pouriran, R. and Nejad, F.R. and Mansoori, N. and Shahmohammadibeni, N. and Taghavi, S. and Shokraeian, P. and Akhavan-Niaki, H. and Paisán-Ruiz, C. and Darvish, H. and Ohadi, M. (2017) Support for "disease-Only" Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in Schizophrenia. Genetic Testing and Molecular Biomarkers.

Andarva, M. and Jamshidi, J. and Ghaedi, H. and Daftarian, N. and Emamalizadeh, B. and Alehabib, E. and Taghavi, S. and Pouriran, R. and Darvish, H. (2017) A novel c.240241insGG mutation in NDP gene in a family with Norrie disease. Clinical and Experimental Optometry.

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