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Genomics|November 1, 1992
Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortiumB J Keats, A A Todorov, L D Atwood, et al.Nature Genetics|September 6, 2000
Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndromeN Katsanis, P L Beales, M O Woods, et al.American Journal of Medical Genetics|March 1, 1994
Clinical diagnosis of the Usher syndromes. Usher Syndrome ConsortiumR J Smith, C I Berlin, J F Hejtmancik, et al.American Journal of Human Genetics|October 1, 1989
Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21D E Merry, J G Lesko, D M Sosnoski, et al.The British Journal of Ophthalmology|July 24, 2001
Evaluation of the G protein coupled receptor-75 (GPR75) in age related macular degenerationC G Sauer, K White, H Stöhr, et al.Nanoscale|November 20, 2015
Mechanism of periodic height variations along self-aligned VLS-grown planar nanostructuresJ A Steele, J Horvat, R A Lewis, et al.Journal of Glaucoma|December 1, 1996
A gene for primary congenital glaucoma is not linked to the locus on chromosome 1q for autosomal dominant juvenile-onset open angle glaucomaK L Anderson, R A Lewis, B A Bejjani, et al.American Journal of Human Genetics|April 16, 1998
Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi ArabiaB A Bejjani, R A Lewis, K F Tomey, et al.Journal of the American Academy of Dermatology|June 1, 1996
Melanoma awareness and self-examination practices: results of a United States surveyD R Miller, A C Geller, S W Wyatt, et al.Neurology|March 14, 2007
CMT1X phenotypes represent loss of GJB1 gene functionM E Shy, C Siskind, E R Swan, et al.Pageof 41