Showing results (331-340 of 365) with videos related to
Sort By:
Pageof 37
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.Human Biology|November 14, 1997
Application of HLA class II polymorphism analysis to the study of the population structure of the Island of Krk, CroatiaI Martinović, M Bakran, A Chaventré, 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.American Journal of Human Genetics|September 29, 2001
Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humansV Berry, P Francis, M A Reddy, et al.The British Journal of Ophthalmology|January 25, 2003
The phenotype of normal tension glaucoma patients with and without OPA1 polymorphismsT Aung, K Okada, D Poinoosawmy, et al.American Journal of Physical Anthropology|November 1, 1987
Isolation by distance in Middle Dalmatia-YugoslaviaP Rudan, D Simić, N Smolej-Narancić, et al.Human Molecular Genetics|December 15, 2000
Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophyS E Wilkie, R J Newbold, E Deery, et al.Pageof 37