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