GJB2 Mutations in Hearing Impairment: Identification of a Broad Clinical Spectrum for Improved Genetic Counseling von Frei, Klemens, Ramsebner, Reinhard, Lucas, Trevor, Hamader, Gertrude, Szuhai, Károly, Weipoltshammer, Klara, Baumgartner, Wolf-Dieter, Wachtler, Franz J., Kirschhofer, Karin

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Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment von Verhoeven, Kristien, Laer, Lut Van, Kirschhofer, Karin, Legan, P. Kevin, Hughes, David C, Schatteman, Isabelle, Verstreken, Margriet, Hauwe, Peter Van, Coucke, Paul, Chen, Achih, Smith, Richard J.H, Somers, Thomas, Offeciers, F. Erwin, Heyning, Paul Van de, Richardson, Guy P, Wachtler, Franz, Kimberling, William J, Willems, Patrick J, Govaerts, Paul J, Camp, Guy Van

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Connexin 26 mutations in cases of sensorineural deafness in eastern Austria von Frei, Klemens, Szuhai, Károly, Lucas, Trevor, Weipoltshammer, Klara, Schöfer, Christian, Ramsebner, Reinhard, Baumgartner, Wolf-Dieter, Raap, Anton K, Bittner, Reginald, Wachtler, Franz J, Kirschhofer, Karin

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High Incidence of GJB2 Mutations During Screening of Newborns for Hearing Loss in Austria von Ramsebner, Reinhard, Volker, Romana, Lucas, Trevor, Hamader, Gertrude, Weipoltshammer, Klara, Baumgartner, Wolf-Dieter, Wachtler, Franz J, Kirschhofer, Karin, Frei, Klemens

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Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern Austria von Frei, Klemens, Ramsebner, Reinhard, Lucas, Trevor, Baumgartner, Wolf-Dieter, Schoefer, Christian, Wachtler, Franz J., Kirschhofer, Karin

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Relevance of the A1555G Mutation in the 12S rRNA Gene for Hearing Impairment in Austria von Ramsebner, Reinhard, Lucas, Trevor, Schoefer, Christian, Ludwig, Martin, Baumgartner, Wolf-Dieter, Wachtler, Franz J, Kirschhofer, Karin, Frei, Klemens

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Relevance of the A1555G mutation in the 12S rRNA gene for hearing impairment in Austria von Ramsebner, Reinhard, Lucas, Trevor, Schoefer, Christian, Ludwig, Martin, Baumgartner, Wolf-Dieter, Wachtler, Franz J, Kirschhofer, Karin, Frei, Klemens

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Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in Austria von Frei, Klemens, Ramsebner, Reinhard, Hamader, Gertrude, Lucas, Trevor, Schoefer, Christian, Baumgartner, Wolf-Dieter, Wachtler, Franz J, Kirschhofer, Karin

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A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness von Frei, Klemens, Lucas, Trevor, Ramsebner, Reinhard, Schöfer, Christian, Baumgartner, Wolf-Dieter, Weipoltshammer, Klara, Erginel-Unaltuna, Nihan, Wachtler, Franz J., Kirschhofer, Karin

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Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family von Kirschhofer, K., Kenyon, J.B., Hoover, D.M., Franz, P., Weipoltshammer, K., Wachtler, F., Kimberling, W.J.

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Differentation of endothelial cells in avian embryos does not depend on gastrulation von Christ, Bodo, Grim, Milos, Wilting, Jörg, Von Kirschhofer, Karin, Wachtler, Franz

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