Hamader G - Search Results

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Identification of a SNP in a regulatory region of GJB2 associated with idiopathic nonsyndromic autosomal recessive hearing loss in a multicenter study.

Ramsebner R, Ludwig M, Lucas T, de Jong D, Hamader G, del Castillo I, Parzefall T, Baumgartner WD, Schoefer C, Szuhai K, Frei K. Ramsebner R, et al. Among authors: hamader g. Otol Neurotol. 2013 Jun;34(4):650-6. doi: 10.1097/MAO.0b013e31828d6501. Otol Neurotol. 2013. PMID: 23640091

Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in Austria.

Frei K, Ramsebner R, Hamader G, Lucas T, Schoefer C, Baumgartner WD, Wachtler FJ, Kirschhofer K. Frei K, et al. Among authors: hamader g. Hear Res. 2004 Aug;194(1-2):81-6. doi: 10.1016/j.heares.2004.03.007. Hear Res. 2004. PMID: 15276679

GJB2 mutations in hearing impairment: identification of a broad clinical spectrum for improved genetic counseling.

Frei K, Ramsebner R, Lucas T, Hamader G, Szuhai K, Weipoltshammer K, Baumgartner WD, Wachtler FJ, Kirschhofer K. Frei K, et al. Among authors: hamader g. Laryngoscope. 2005 Mar;115(3):461-5. doi: 10.1097/01.mlg.0000157855.47143.71. Laryngoscope. 2005. PMID: 15744158

High incidence of GJB2 mutations during screening of newborns for hearing loss in Austria.

Ramsebner R, Volker R, Lucas T, Hamader G, Weipoltshammer K, Baumgartner WD, Wachtler FJ, Kirschhofer K, Frei K. Ramsebner R, et al. Among authors: hamader g. Ear Hear. 2007 Jun;28(3):298-301. doi: 10.1097/AUD.0b013e318047932d. Ear Hear. 2007. PMID: 17485979

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