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Chapi, Marjan and Sabbaghi, Hamideh and Suri, Fatemeh and Alehabib, Elham and Rahimi-Aliabadi, Simin and Jamali, Faezeh and Jamshidi, Javad and Emamalizadeh, Babak and Darvish, Hossein and Mirrahimi, Mehraban and Ahmadieh, Hamid and Daftarian, Narsis (2019) Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy. OPHTHALMIC GENETICS, 40 (3). pp. 259-266.
Safarpour Lima, Behnam and Ghaedi, Hamid and Daftarian, Narsis and Ahmadieh, Hamid and Jamshidi, Javad and Khorrami, Mehdi and Noroozi, Rezvan and Sohrabifar, Nasim and Assarzadegan, Farhad and Hesami, Omid and Taghavi, Shaghayegh and Ahmadifard, Azadeh and Atakhorrami, Minoo and Rahimi-Aliabadi, Simin and Shahmohammadibeni, Neda and Alehabib, Elham and Andarva, Monavvar and Darvish, Hossein and Emamalizadeh, Babak (2016) c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness. European journal of medical genetics, 59 (2). pp. 65-9. ISSN 1878-0849
