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Publications by Jurklies, B.

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Number of items: 5.


Sauer, C. G., White, K., Kellner, U., Rudolph, G., Jurklies, B., Pauleikhoff, D. and Weber, Bernhard H. F. (2001) EFEMP1 is not associated with sporadic early onset drusen. Ophthalmic Genetics 22, pp. 27-34. Fulltext not available.


Rivera, A., White, K., Stöhr, H., Steiner, K., Hemmrich, N., Grimm, T., Jurklies, B., Lorenz, B., Scholl, H. P. N., Apfelstedt-Sylla, E. and Weber, Bernhard H. F. (2000) A Comprehensive Survey of Sequence Variation in the ABCA4 (ABCR) Gene in Stargardt Disease and Age-Related Macular Degeneration. The American Journal of Human Genetics 67 (4), pp. 800-813. Fulltext not available.

Krämer, F., White, K., Pauleikhoff, D., Gehrig, A., Passmore, L., Rivera, A., Rudolph, G., Kellner, U., Andrassi, M., Lorenz, B., Rohrschneider, K., Blankenagel, A., Jurklies, B., Schilling, H., Schütt, F., Holz, F. G. and Weber, Bernhard H. F. (2000) Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration. European Journal of Human Genetics 8 (4), pp. 286-292. Fulltext not available.


Stöhr, H., Klein, J., Gehrig, A., Koehler, M. R., Jurklies, B., Kellner, U., Leo-Kottler, B., Schmid, M. and Weber, Bernhard H. F. (1999) Mapping and genomic characterization of the gene encoding diacylglycerol kinase γ (DAGK3): assessment of its role in dominant optic atrophy (OPA1). Human Genetics 104 (1), pp. 99-105. Fulltext not available.


Sauer, G. S., Gehrig, A., Warneke-Wittstock, R., Marquardt, A., Ewing, C. C., Gibson, A., Lorenz, B., Jurklies, B. and Weber, Bernhard H. F. (1997) Positional cloning of the gene associated with X-linked juvenile retinoschisis. Nature Genetics 17, pp. 164-170. Fulltext not available.

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