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Investigative Ophthalmology & Visual Science|March 1, 1997
Retinoschisislike alterations in the mouse eye caused by gene targeting of the Norrie disease geneK Ruether, D van de Pol, G Jaissle, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|April 22, 2019
A case of X-linked retinoschisis with atypical fundus appearanceF Nasser, S Kohl, L Kuehlewein, et al.
Investigative Ophthalmology & Visual Science|October 3, 2001
Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX geneH P Scholl, H Langrová, C M Pusch, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 29, 1997
Ocular findings in patients with autosomal dominant retinitis pigmentosa and Cys110Phe, Arg135Gly, and Gln344stop mutations of rhodopsinS Kremmer, A Eckstein, A Gal, et al.
American Journal of Human Genetics|March 1, 1992
Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsinC J Weitz, Y Miyake, K Shinzato, et al.
Human Genetics|September 12, 2000
Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1F K Jacobi, M Broghammer, K Pesch, et al.
Vox Sanguinis|January 1, 1989
A new HLA-B antigen, BHT: definition by serological and biochemical meansA Hajek-Rosenmayr, L Jungl, M Kirnbauer, et al.
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