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Publications by Foerster, M H

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Number of items: 3.


Renner, A B, Kellner, U, Fiebig, B, Cropp, E, Foerster, M H and Weber, Bernhard H. F. (2008) ERG variability in X-linked congenital retinoschisis patients with mutations in the RS1 gene and the diagnostic importance of fundus autofluorescence and OCT. Documenta Ophthalmologica 116 (2), pp. 97-109. Fulltext not available.


Renner, A B, Tillack, H, Kraus, H, Kramer, F, Mohr, N, Weber, Bernhard H. F. , Foerster, M H and Kellner, U (2005) Late Onset is Common in Best Macular Dystrophy Associated with VMD2 Gene Mutations. Ophthalmology 112 (4), pp. 586-592. 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.

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