AAAAAA

   
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: Nekahm, D Pototschnig, C Thumfart, WF
Citation: D. Nekahm et al., Functional disorders of the oesophagus and their manifestations in the ENTregion, LARY RH OTO, 77(11), 1998, pp. 640-641
Risultati: 1-4 |