Authors: Jung, HH Hergersberg, M Kneifel, S Alkadhi, H Schiess, R Weigell-Weber, M Daniels, G Kollias, S Hess, K

Citation: Hh. Jung et al., McLeod syndrome: A novel mutation, predominant psychiatric manifestations,and distinct striatal imaging findings, ANN NEUROL, 49(3), 2001, pp. 384-392

Authors: Weigell-Weber, M Schinzel, A Hergersberg, M

Citation: M. Weigell-weber et al., Hereditary hearing loss due to mutations in the connexin-26 gene, SCHW MED WO, 130(29-30), 2000, pp. 1072-1077

Authors: Hergersberg, M Weigell-Weber, M

Citation: M. Hergersberg et M. Weigell-weber, Inherited hearing loss: new diagnostic possibilities, SCHW MED WO, 130(13), 2000, pp. 485-489

Authors: Weigell-Weber, M Fokstuen, S Torok, B Niemeyer, G Schinzel, A Hergersberg, M

Citation: M. Weigell-weber et al., Codons 837 and 838 in the retinal guanylate cyclase gene on chromosome 17p: Hot spots for mutations in autosomal dominant cone-rod dystrophy?, ARCH OPHTH, 118(2), 2000, pp. 300-300

Authors: Laccone, F Engel, U Holinski-Feder, E Weigell-Weber, M Marczinek, K Nolte, D Morris-Rosendahl, DJ Zuhlke, C Fuchs, K Weirich-Schwaiger, H Schluter, G von Beust, G Vieira-Saecker, AMM Weber, BHF Riess, O

Citation: F. Laccone et al., DNA analysis of Huntington's disease - Five years of experience in Germany, Austria, and Switzerland, NEUROLOGY, 53(4), 1999, pp. 801-806