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Publications by Grimm, T

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Jump to: 2013 | 2010 | 2001 | 2000 | 1997 | 1996
Number of items: 7.

2013

Stellzig-Eisenhauer, A, Decker, E, Meyer-Marcotty, P, Rau, C, Fiebig, B S, Kress, W, Saar, K, Rüschendorf, F, Hubner, N, Grimm, T, Witt, E and Weber, Bernhard H. F. (2013) [Primary failure of eruption (PFE). Clinical and molecular genetics analysis] Article in French. L' orthodontie française 84 (3), pp. 241-250. Fulltext not available.

2010

Stellzig-Eisenhauer, A, Decker, E, Meyer-Marcotty, P, Rau, C, Fiebig, B S, Kress, W, Saar, K, Rüschendorf, F, Hubner, N, Grimm, T, Witt, E and Weber, Bernhard H. F. (2010) Primary failure of eruption (PFE)--clinical and molecular genetics analysis. Journal of Orofacial Orthopedics/Fortschritte der Kieferorthopädie 71 (1), pp. 6-16. Fulltext not available.

2001

Sauer, C G, White, K, Stöhr, H, Grimm, T, Hutchinson, A, Bernstein, P S, Lewis, R A, Simonelli, F, Pauleikhoff, D, Allikmets, R and Weber, Bernhard H. F. (2001) Evaluation of the G protein coupled receptor-75 (GPR75) in age related macular degeneration. British Journal of Ophthalmology 85 (8), pp. 969-975. Fulltext not available.

2000

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.

Hofferbert, S, Worringen, U, Backe, J, Rückert, E-M, White, K, Faller, H, Grimm, T, Caffier, H, Chang-Claude, J and Weber, Bernhard H. F. (2000) Simultaneous Interdisciplinary counseling in germany breast/ovarian cancer families: first experiences with patient perceptions, surveillance behavior and acceptance of genetic testing. Genetic Counseling 11, pp. 127-146. Fulltext not available.

1997

Sauer, C G, Schworm, H D, Ulbig, M, Blankenagel, A, Rohrschneider, K, Pauleikhoff, D, Grimm, T and Weber, Bernhard H. F. (1997) An ancestral core haplotype defines the critical region harbouring the North Carolina macular dystrophy gene (MCDR1). Journal of Medical Genetics 34 (12), pp. 961-966. 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.

This list was generated on Wed Sep 18 15:27:38 2019 CEST.
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