A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran
Babanejad, Mojgan, Fattahi, Zohreh, Bazazzadegan, Niloofar, Nishimura, Carla, Meyer, Nicole, Nikzat, Nooshin, Sohrabi, Elahe, Najmabadi, Amin, Jamali, Peyman, Habibi, Farkhonde, Smith, Richard J.H., Kahrizi, Kimia, Najmabadi, Hossein
Published in American journal of medical genetics. Part A (01.10.2012)
Published in American journal of medical genetics. Part A (01.10.2012)
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Journal Article
Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran
Mohseni, Marzieh, Babanejad, Mojgan, Booth, Kevin T., Jamali, Payman, Jalalvand, Khadijeh, Davarnia, Behzad, Ardalani, Fariba, Khoshaeen, Atefeh, Arzhangi, Sanaz, Ghodratpour, Fatemeh, Beheshtian, Maryam, Jahanshad, Faezeh, Otukesh, Hasan, Bahrami, Fatemeh, Seifati, Seyed Morteza, Bazazzadegan, Niloofar, Habibi, Farkhonde, Behravan, Hanieh, Mirzaei, Sepide, Keshavarzi, Fatemeh, Nikzat, Nooshin, Mehrjoo, Zohreh, Thiele, Holger, Nothnagel, Michael, Azaiez, Hela, Smith, Richard J., Kahrizi, Kimia, Najmabadi, Hossein
Published in Clinical genetics (01.07.2021)
Published in Clinical genetics (01.07.2021)
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Journal Article