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Results: 1-4 |
Results: 4

Authors: Loffler, J Nekahm, D Hirst-Stadlmann, A Gunther, B Menzel, HJ Utermann, G Janecke, AR
Citation: J. Loffler et al., Sensorineural hearing loss and the incidence of Cx26 mutations in Austria, EUR J HUM G, 9(3), 2001, pp. 226-230

Authors: Janecke, AR Nekahm, D Loffler, J Hirst-Stadlmann, A Muller, T Utermann, G
Citation: Ar. Janecke et al., De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing loss, HUM GENET, 108(3), 2001, pp. 269-270

Authors: Nekahm, D Weichbold, V Welzl-Mueller, K Hirst-Stadlmann, A
Citation: D. Nekahm et al., Improvement in early detection of congenital hearing impairment due to universal newborn hearing screening, INT J PED O, 59(1), 2001, pp. 23-28

Authors: Haberlandt, E Loffler, J Hirst-Stadlmann, A Stockl, B Judmaier, W Fischer, H Heinz-Erian, P Muller, T Utermann, G Smith, RJH Janecke, AR
Citation: E. Haberlandt et al., Split hand/split foot malformation associated with sensorineural deafness,inner and middle ear malformation, hypodontia, congenital vertical talus, and deletion of eight microsatellite markers in 7q21.1-q21.3, J MED GENET, 38(6), 2001, pp. 405-409
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