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Hospital Practice (1995)|July 8, 2000
Macular degeneration: the emerging geneticsR A Lewis, J R LupskiAmerican Journal of Ophthalmology|June 1, 2001
Analysis of the ABCR (ABCA4) gene in 4-aminoquinoline retinopathy: is retinal toxicity by chloroquine and hydroxychloroquine related to Stargardt disease?N F Shroyer, R A Lewis, J R LupskiHuman Genetics|April 4, 2000
Complex inheritance of ABCR mutations in Stargardt disease: linkage disequilibrium, complex alleles, and pseudodominanceN F Shroyer, R A Lewis, J R LupskiOphthalmology|July 1, 1996
Ophthalmic manifestations of Smith-Magenis syndromeR M Chen, J R Lupski, F Greenberg, et al.Human Genetics|May 31, 2001
Late-onset Stargardt disease is associated with missense mutations that map outside known functional regions of ABCR (ABCA4)A N Yatsenko, N F Shroyer, R A Lewis, et al.Investigative Ophthalmology & Visual Science|November 1, 2001
Null missense ABCR (ABCA4) mutations in a family with stargardt disease and retinitis pigmentosaN F Shroyer, R A Lewis, A N Yatsenko, et al.American Journal of Human Genetics|April 1, 1992
Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacyL Pentao, R A Lewis, D H Ledbetter, et al.Nature Genetics|May 1, 1994
Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneousM Leppert, L Baird, K L Anderson, et al.Human Molecular Genetics|December 1, 2001
Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degenerationN F Shroyer, R A Lewis, A N Yatsenko, et al.Trends in Genetics : TIG|November 20, 1998
Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traitsJ R LupskiPageof 56