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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: Witsch-Raumgartner, M Ciara, E Loffler, J Menzel, HJ Seedorf, U Burn, J Gillessen-Kaesbach, G Hoffmann, GF Fitzy, BU Mundy, H Clayton, P Kelley, RI Krajewska-Walasek, M Utermann, G
Citation: M. Witsch-raumgartner et al., Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutations, EUR J HUM G, 9(1), 2001, pp. 45-50

Authors: Witsch-Baumgartner, M Loeffler, J Menzel, HJ Utermann, G Neuhaus, C
Citation: M. Witsch-baumgartner et al., Mutation screening in the DHCR7 gene of patients with attention deficit and hyperactivity disorder, AM J MED G, 102(1), 2001, pp. 106-107

Authors: Kronenberg, MF Menzel, HJ Ebersbach, G Wenning, GK Luginger, E Gollner, M Ransmayr, G Utermann, G Poewe, W Kronenberg, F
Citation: Mf. Kronenberg et al., Dopamine D4 receptor polymorphism and idiopathic Parkinson's disease, EUR J HUM G, 7(3), 1999, pp. 397-400
Risultati: 1-4 |