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

By Chinetti Viviana   Iossa Sandra   Auletta Gennaro   Laria Carla   de Luca Maria   Leva Francesca Di   Riccardi Pasquale   Giannini Pasquale   Gasparini Paolo   Ciccodicola Alfredo   Marciano Elio   Franzè Annamaria  

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

Informa Healthcare

Access to resources Recommend Favorite

Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6 digenic inheritance in a large Italian cohort

By Cama Elona   Melchionda Salvatore   Palladino Teresa   Carella Massimo   Santarelli Rosamaria   Genovese Elisabetta   Benettazzo Filippo   Zelante Leopoldo   Arslan Edoardo  

International Journal of Audiology, Vol. 48, Iss. 1, 2009-01 ,pp. : 12-17

Informa Healthcare

Access to resources Recommend Favorite

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

Informa Healthcare

Access to resources Recommend Favorite

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

Informa Healthcare

Access to resources Recommend Favorite

Prevalence and risk factors for mild and high-frequency bilateral sensorineural hearing loss at age 11 years old: A UK prospective cohort study

By Hall Amanda J.   Midgley Elizabeth   Steer Colin   Humphriss Rachel  

International Journal of Audiology, Vol. 50, Iss. 11, 2011-11 ,pp. : 809-814

Informa Healthcare

Access to resources Recommend Favorite