A novel mutation in the FOXC1 gene in a family with Axenfeld-Rieger syndrome and Peters' anomalyWEISSCHUH, N; WOLF, C; WISSINGER, B et al.Clinical genetics. 2008, Vol 74, Num 5, pp 476-480, issn 0009-9163, 5 p.Article

Morphology of the sella turcica in Axenfeld-Rieger syndrome with PITX2 mutationMEYER-MARCOTTY, P; WEISSCHUH, N; DRESSLER, P et al.Journal of oral pathology & medicine. 2008, Vol 37, Num 8, pp 504-510, issn 0904-2512, 7 p.Article

Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosaSCHUSTER, A; WEISSCHUH, N; JÄGLE, H et al.British journal of ophthalmology. 2005, Vol 89, Num 10, pp 1258-1264, issn 0007-1161, 7 p.Article