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Journal of Neurology|February 1, 1993
The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalitiesK M Bushby, D Gardner-Medwin, L V Nicholson, et al.Human Genetics|March 10, 1999
Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD)S Kermani, K Gregory-Evans, E E Tarttelin, et al.Investigative Ophthalmology & Visual Science|October 23, 1997
Single exposures to antiproliferatives: long-term effects on ocular fibroblast wound-healing behaviorN L Occleston, J T Daniels, R W Tarnuzzer, et al.Human Gene Therapy|February 11, 1998
Adeno-associated virus gene transfer to mouse retinaR R Ali, M B Reichel, M De Alwis, et al.The British Journal of Ophthalmology|May 23, 2006
Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk geneM Tschernutter, S A Jenkins, N H Waseem, et al.Journal of Medical Genetics|July 1, 1991
Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindredA F Wright, S S Bhattacharya, M A Aldred, et al.The British Journal of Ophthalmology|October 27, 2007
Sequencing of the CHST6 gene in Czech macular corneal dystrophy patients supports the evidence of a founder mutationP Liskova, B Veraitch, K Jirsova, et al.Annals of Human Genetics|December 13, 2006
A novel genetic study of Chinese families with autosomal recessive retinitis pigmentosaM M Abd El-Aziz, M F El-Ashry, W M Chan, et al.American Journal of Human Genetics|September 1, 1990
Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneityD H Lester, C F Inglehearn, R Bashir, et al.Current Eye Research|September 24, 1998
Absence of p53 delays apoptotic photoreceptor cell death in the rds mouseR R Ali, M B Reichel, N Kanuga, et al.Pageof 18