Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient von Taghdiri, Maryam, Kashef, Atie, Abbassi, Golemaryam, Moshtagh, Azadeh, Sadatian, Neda, Fardaei, Majid, Najafi, Kimia, Kariminejad, Roxana

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Identification of a novel deletion within ALDH3A2 gene in an Iranian Family with Sjögren–Larsson Syndrome von Taghdiri, Maryam, Kashef, Atie, Fardaei, Majid, Miryounesi, Mohammad

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A novel mutation of the USH2C (GPR98) gene in an Iranian family with Usher syndrome type II von KAHRIZI, KIMIA, BAZAZZADEGAN, NILOOFAR, JAMALI, LEILA, NIKZAT, NOOSHIN, KASHEF, ATIE, NAJMABADI, HOSSEIN

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

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Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of Hearing Loss in Iranian population von Kashef, Atie, Nikzat, Nooshin, Bazzazadegan, Niloofar, Fattahi, Zohreh, Sabbagh-Kermani, Farahnaz, Taghdiri, Maryam, Azadeh, Batool, Mojahedi, Faezeh, Khoshaeen, Atefeh, Habibi, Haleh, Najmabadi, Hossein, Kahrizi, Kimia

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Identification of a novel deletion within ALDH3A2 gene in an Iranian Family with Sjögren-Larsson Syndrome von Taghdiri, Maryam, Kashef, Atie, Fardaei, Majid, Miryounesi, Mohammad

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Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient von Taghdiri, Maryam, Kashef, Atie, Abbassi, Golemaryam, Moshtagh, Azadeh, Sadatian, Neda, Fardaei, Majid, Najafi, Kimia, Kariminejad, Roxana

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