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  1. 1
    Hossein Najmabadi, Kimia Kahrizi, Genetics of non-syndromic hearing loss in the Middle East, International Journal of Pediatric Otorhinolaryngology, 2014, 78, 12, 2026

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  2. 2
    Lies H Hoefsloot, Anne-Françoise Roux, Maria Bitner-Glindzicz, EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus, European Journal of Human Genetics, 2013, 21, 11, 1325

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    Niloofar Bazazzadegan, Nooshin Nikzat, Zohreh Fattahi, Carla Nishimura, Nicole Meyer, Shima Sahraian, Payman Jamali, Mojgan Babanejad, Atie Kashef, Hilda Yazdan, Farahnaz Sabbagh Kermani, Maryam Taghdiri, Batool Azadeh, Faezeh Mojahedi, Atefeh Khoshaeen, Haleh Habibi, Farahnaz Reyhanifar, Narges Nouri, Richard J.H. Smith, Kimia Kahrizi, Hossein Najmabadi, The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss—A twelve year study, International Journal of Pediatric Otorhinolaryngology, 2012, 76, 8, 1164

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