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Publications by Wissinger, B

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Number of items: 4.


Renner, A B, Fiebig, B, Weber, Bernhard H. F. , Wissinger, B, Andreasson, S, Gal, A, Cropp, E, Kohl, S and Kellner, U (2009) Phenotypic variability and long-term follow-up of patients with known and novel PRPH2/RDS gene mutations. American Journal of Ophthalmology 147 (3), pp. 518-530. Fulltext not available.


Renner, A B, Tillack, H, Kraus, H, Kohl, S, Wissinger, B, Mohr, N, Weber, Bernhard H. F. , Kellner, U and Foerster, M H (2004) Morphology and Functional Characteristics in Adult Vitelliform Macular Dystrophy. Retina 24 (6), pp. 929-939. Fulltext not available.


Wutz, K, Sauer, C, Zrenner, E, Lorenz, B, Alitalo, T, Broghammer, M, Hergersberg, M, de La Chapelle, A, Weber, Bernhard H. F. , Wissinger, B, Meindl, A and Pusch, C M (2002) Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina. European Journal of Human Genetics 10 (8), pp. 449-456. Fulltext not available.


Weber, Bernhard H. F. , Sander, S, Kopp, C, Walker, D, Eckstein, A, Wissinger, B, Zrenner, E and Grimm, T (1996) Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of cases. British Journal of Ophthalmology 80 (8), pp. 745-749. Fulltext not available.

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