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Eye (London, England)|November 7, 2009
Long-term follow-up of a family with dominant X-linked retinitis pigmentosaD M Wu, H Khanna, P Atmaca-Sonmez, et al.Human Heredity|July 1, 1996
Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American familyY C Hou, J E Richards, E L Bingham, et al.Genomics|March 2, 1999
Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22S M Walpole, K T Hiriyana, A Nicolaou, et al.American Journal of Human Genetics|September 6, 2000
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15A J Mears, S Hiriyanna, R Vervoort, et al.British Journal of Urology|August 1, 1986
Metabolic consequences of forced diuresis following prostatectomyP R Malone, J H Davies, N J Standfield, et al.Journal of Public Health Management and Practice : JPHMP|April 7, 1997
The presence of total quality management and continuous quality improvement processes in California public health clinicsF D Scutchfield, M L Zúñiga de Nuncio, R A Bush, et al.American Journal of Human Genetics|July 1, 1996
A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3R Fujita, E Bingham, P Forsythe, et al.Genomics|May 20, 1999
Bestrophin gene mutations in patients with Best vitelliform macular dystrophyG M Caldwell, L E Kakuk, I B Griesinger, et al.Investigative Ophthalmology & Visual Science|November 30, 2000
Genetics and phenotypes of RPE65 mutations in inherited retinal degenerationD A Thompson, P Gyürüs, L L Fleischer, et al.Journal of Epidemiology and Community Health|May 20, 2000
Epidemiology of participation: an Australian community studyF E Baum, R A Bush, C C Modra, et al.Pageof 10