Entries of Wissinger, B. on the publication server
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Number of items: 4.
2009
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.
, 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.
2004
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.
, 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.
2002
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.
, 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.
1996
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.
, 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.