Showing results (111-120 of 178) with videos related to
Sort By:
Pageof 18
Environmental Pollution (Barking, Essex : 1987)|November 22, 2015
The effects of composting approaches on the emissions of anthropogenic volatile organic compounds: A comparison between vermicomposting and general aerobic compostingS S Bhattacharya, Ki-Hyun Kim, Md Ahsan Ullah, et al.Eye (London, England)|March 16, 2004
BIGH3 mutation in a Bangladeshi family with a variable phenotype of LCDIM F El-Ashry, M M Abd El-Aziz, L A Ficker, et al.Molecular Vision|August 4, 2006
A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic familyP K F Addison, V Berry, K R Holden, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|February 7, 2001
Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1S M Downes, G E Holder, F W Fitzke, et al.Journal of Medical Genetics|February 25, 1998
A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneityC F Inglehearn, E E Tarttelin, C Plant, et al.Genome Research|February 1, 1996
Sorsby's fundus dystrophy in the British Isles: demonstration of a striking founder effect by microsatellite-generated haplotypesS D Wijesuriya, K Evans, M R Jay, et al.Human Genetics|September 10, 1999
Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locusI Zito, D L Thiselton, M B Gorin, et al.The British Journal of Ophthalmology|August 1, 1993
Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic studyA T Moore, F Fitzke, M Jay, et al.Human Molecular Genetics|February 1, 1994
Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19M al-Maghtheh, C F Inglehearn, T J Keen, et al.The British Journal of Ophthalmology|January 1, 1995
Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expressionR Y Kim, F W Fitzke, A T Moore, et al.Pageof 18