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Publications by Walker, D

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Jump to: 1996 | 1994
Number of items: 5.

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.

1994

Weber, Bernhard H. F. , Stöhr, H and Walker, D (1994) A Case of Nonpenetrance in Best's Disease. American Journal of Ophthalmology 118 (3), pp. 398-399. Fulltext not available.

Weber, Bernhard H. F. , Walker, D, Müller, B and Mar, L (1994) Best's Vitelliform Dystrophy (VMD2) Maps between D11S903 and PYGM: No Evidence for Locus Heterogeneity. Genomics 20 (2), pp. 267-274. Fulltext not available.

Weber, Bernhard H. F. , Vogt, G, Stöhr, H, Sander, S, Walker, D and Jones, C (1994) High-resolution meiotic and physical mapping of the best vitelliform macular dystrophy (VMD2) locus to pericentromeric chromosome 11. The American Journal of Human Genetics 55 (6), pp. 1182-1187. Fulltext not available.

Weber, Bernhard H. F. , Walker, D and Müller, B (1994) Molecular evidence for non-penetrance in Best's disease. Journal of Medical Genetics 31 (5), pp. 388-392. Fulltext not available.

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