Search Results - Rodbaneh, Ehsan Abbaspour

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    GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran

    GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran by Abbaspour Rodbaneh, Ehsan, Panahi, Mohammad, Rahimi, Bahareh, Mokabber, Haleh, Farajollahi, Reza, Davarnia, Behzad

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    De novo KAT6B mutation causes Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome in an Iranian boy: a case report

    De novo KAT6B mutation causes Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome in an Iranian boy: a case report by Davarnia, Behzad, Panahi, Mohammad, Rahimi, Bahareh, Anari, Hassan, Farajollahi, Reza, Rodbaneh, Ehsan Abbaspour, Jeddi, Farhad

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