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The British Journal of Ophthalmology|July 1, 1995
Efficient DNA carrier detection in X linked juvenile retinoschisisA A Bergen, J B ten Brink, M J van SchooneveldGene Therapy|March 11, 2026
AAV-mediated gene replacement therapy for LRAT-associated retinitis pigmentosa: a proof-of-concept study in a patient-based rat modelA M El-Kalaani, J B Ten Brink, C J F Boon, et al.Human Molecular Genetics|May 1, 1995
Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene regionA A Bergen, J B ten Brink, F Riemslag, et al.Journal of Medical Genetics|December 1, 1994
Refinement of the chromosomal position of the X linked juvenile retinoschisis geneA A Bergen, J B ten Brink, L M Bleeker-Wagemakers, et al.Journal of Medical Genetics|October 1, 1996
Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1A A Bergen, J B ten Brink, F Riemslag, et al.The British Journal of Ophthalmology|June 30, 2000
Sorsby fundus dystrophy without a mutation in the TIMP-3 geneJ J Assink, E de Backer, J B ten Brink, et al.American Journal of Human Genetics|October 23, 1997
A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosomeJ J Assink, N T Tijmes, J B ten Brink, et al.Journal of Medical Genetics|November 8, 2005
Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosaJ C Booij, R J Florijn, J B ten Brink, et al.Nature Genetics|June 3, 2000
Mutations in ABCC6 cause pseudoxanthoma elasticumA A Bergen, A S Plomp, E J Schuurman, et al.Stem Cell Reviews and Reports|July 22, 2017
Stem Cell Derived Retinal Pigment Epithelium: The Role of Pigmentation as Maturation Marker and Gene Expression Profile Comparison with Human Endogenous Retinal Pigment EpitheliumA Bennis, J G Jacobs, L A E Catsburg, et al.Pageof 2