Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder

by Francesca Mattioli, Hossein Darvish, Sohail Aziz Paracha, Abbas Tafakhori, Saghar Ghasemi Firouzabadi, Marjan Chapi, Hafiz Muhammad Azhar Baig, Alexandre Reymond, Stylianos E. Antonarakis, Muhammad Ansar
Published 2021-11-01

Genetic Causes of Mental Retardation in Golestan Province

by Hossein Darvish, Saghar Ghasemi-Firouzabadi, Gholam Reza Bahrami-Monajemi, Ideh Bahman, Marziyeh Mohseni, Mohammad Javad Soltani-Banavandi, Sousan Banihashemi , Sanaz Arjangi, Farkhondeh Behjati, Kimia Kahrizi, Hossein Najmabadi
Published 2010-10-01

Investigation of Chromosomal Abnormalities and Microdeletion/Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies

by Akbar Mohammadzadeh, Susan Akbaroghli, Ehsan Aghaei-Moghadam, Nejat Mahdieh, Reza Shervin Badv, Payman Jamali, Roxana Kariminejad, Zahra Chavoshzadeh, Saghar Ghasemi Firouzabadi, Roxana Mansour Ghanaie, Ahoura Nozari, Sussan Banihashemi, Fatemeh Hadipour, Zahra Hadipour, Ariana Kariminejad, Hossein Najmabadi, Yousef Shafeghati, Farkhondeh Behjati
Published 2019-06-01