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Ophthalmic Genetics|November 12, 1998
ABCR unites what ophthalmologists divide(s)M A van Driel, A Maugeri, B J Klevering, et al.IEEE Transactions on Visualization and Computer Graphics|April 29, 2020
Visual Analytics for Hypothesis-Driven Exploration in Computational PathologyA Corvo, H S Garcia Caballero, M A Westenberg, et al.Nucleic Acids Research|June 28, 2005
GeneSeeker: extraction and integration of human disease-related information from web-based genetic databasesM A van Driel, K Cuelenaere, P P C W Kemmeren, et al.Genomics|June 22, 1999
Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridizationA I den Hollander, M A van Driel, Y J de Kok, et al.Scientific Reports|September 10, 2017
Complete sequence-based pathway analysis by differential on-chip DNA and RNA extraction from a single cellD van Strijp, R C M Vulders, N A Larsen, et al.American Journal of Human Genetics|March 26, 1999
The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt diseaseA Maugeri, M A van Driel, D J van de Pol, et al.Nature Genetics|October 3, 1999
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)A I den Hollander, J B ten Brink, Y J de Kok, et al.Pageof 1