Search Results - "Zarrintaj Keihanidoust"

"Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes by Rafati, Maryam, Seyyedaboutorabi, Elaheh, Ghadirzadeh, Mohammad R, Heshmati, Yaser, Adibi, Homeira, Keihanidoust, Zarrintaj, Eshraghian, Mohammad R, Javadi, Gholam Reza, Dastan, Jila, Mosavi-Jarrahi, Alireza, Hoseini, Azadeh, Purhoseini, Marzieh, Ghaffari, Saeed R

“…Interstitial Microdeletion and Microduplication syndromes have been proposed as a significant cause of sporadic intellectual disability (ID) but the role of…”
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"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements by Rafati, Maryam, Ghadirzadeh, Mohammad R, Heshmati, Yaser, Adibi, Homeira, Keihanidoust, Zarrintaj, Eshraghian, Mohammad R, Dastan, Jila, Hoseini, Azadeh, Purhoseini, Marzieh, Ghaffari, Saeed R

“…Cryptic subtelomeric rearrangements have been proposed as a significant cause of sporadic intellectual disability (ID) but the role of such aberrations in…”
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Vitamin D deficiency in school-age Iranian children with attention-deficit/hyperactivity disorder (ADHD) symptoms: A critical comparison with healthy controls by Fasihpour, Bahareh, Moayeri, Heshmat, Shariat, Mamak, Keihanidoust, Zarrintaj, Effatpanah, Mohammad, Khedmat, Leila

“…The associations between serum vitamin D levels and the severity of attention-deficit/hyperactivity disorder (ADHD) symptoms were assessed among Iranian…”
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Long QT in children with congenital deafness: a brief report by Naseraldin Akbari Asbagh, Parvin Akbari Asbagh, Zarrintaj Keihanidoust, Aliashraf Eghbali

“…Background: Long QT syndromes (LQT) are genetic abnormalities of ventricular repo-larization, with an estimated incidence of about one per 10000 births. It is…”
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