Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing loss

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International Journal of Audiology, Vol. 49, Iss. 4, 2010-03 ,pp. : 326-331

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Spectrum and frequency of GJB2 mutations in a cohort of 264 Portuguese nonsyndromic sensorineural hearing loss patients

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International Journal of Audiology, Vol. 52, Iss. 7, 2013-07 ,pp. : 466-471

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GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population

By Khalifa Alkowari M.   Girotto G.   Abdulhadi K.   Dipresa S.   Siam R.   Najjar N.   Badii R.   Gasparini P.  

International Journal of Audiology, Vol. 51, Iss. 3, 2012-03 ,pp. : 181-185

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Mutational analysis for GJB2, GJB6, and GJB3 genes in Campania within a universal neonatal hearing screening programme

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International Journal of Audiology, Vol. 50, Iss. 12, 2011-12 ,pp. : 866-870

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GJB2 (Connexin-26) mutations are not frequent among hearing impaired patients in East Greenland

By Homøe Preben   Koch Anders   Rendtorff Nanna Dahl   Lodahl Marianne   Andersen Ture   Andersen Stig   Eiberg Hans   Nielsen Inge-Merete   Tranebjærg Lisbeth  

International Journal of Audiology, Vol. 51, Iss. 6, 2012-06 ,pp. : 433-436

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