Number of items: 6.
2007
Reinhard, J.,
Messias, A.,
Dietz, K.,
Mackeben, M.,
Lakmann, R.,
Scholl, H. P.,
Apfelstedt-Sylla, E.,
Weber, Bernhard H. F. ,
Seeliger, M. W.,
Zrenner, E. and
Trauzettel-Klosinski, S.
(2007)
Quantifying fixation in patients with Stargardt disease.
Vision Research 47 (15), pp. 2076-2085.
Fulltext not available.
2002
2001
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.
1998
Strom, T. M.,
Nyakatura, G.,
Apfelstedt-Sylla, E.,
Hellebrand, H.,
Lorenz, B.,
Weber, Bernhard H. F. ,
Wutz, K.,
Gutwillinger, N.,
Rüther, K.,
Drescher, B.,
Sauer, C. G.,
Zrenner, E.,
Meitinger, T.,
Rosenthal, A. and
Meindl, A.
(1998)
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
Nature Genetics 19, pp. 260-263.
Fulltext not available.
1996
Felbor, U.,
Stöhr, H.,
Amann, T.,
Schönherr, U.,
Apfelstedt-Sylla, E. and
Weber, Bernhard H. F.
(1996)
A second independent Tyr168Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy.
Journal of Medical Genetics 33 (3), pp. 233-236.
Fulltext not available.
This list was generated on Thu Nov 14 02:56:53 2024 CET.