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Human Genetics|October 1, 1986
Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 (L1.28): further linkage data, heterogeneity testing, and risk estimationJ F Clayton, A F Wright, M Jay, et al.Bioresource Technology|June 8, 2014
Vermicomposting of Tea Factory Coal Ash: metal accumulation and metallothionein response in Eisenia fetida (Savigny) and Lampito mauritii (Kinberg)L Goswami, S Sarkar, S Mukherjee, et al.Investigative Ophthalmology & Visual Science|March 11, 2000
A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13A Hameed, S Khaliq, M Ismail, et al.Human Genetics|December 6, 2001
A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effectD L Thiselton, C Alexander, A Morris, et al.Human Genetics|January 1, 1992
Localisation of the gene for Norrie disease to between DXS7 and DXS426 on XpS Lindsay, D L Thiselton, J B Bateman, et al.Human Molecular Genetics|May 1, 1996
Gene transfer into the mouse retina mediated by an adeno-associated viral vectorR R Ali, M B Reichel, A J Thrasher, et al.Human Molecular Genetics|March 21, 1998
A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1A M Payne, S M Downes, D A Bessant, et al.Genome Research|November 1, 1996
Mapping the RP2 locus for X-linked retinitis pigmentosa on proximal Xp: a genetically defined 5-cM critical region and exclusion of candidate genes by physical mappingD L Thiselton, R M Hampson, M Nayudu, et al.Human Genetics|December 1, 1991
Identification of a mutation in the promoter region of the dystrophin gene in a patient with atypical Becker muscular dystrophyK M Bushby, N J Cleghorn, A Curtis, et al.American Journal of Human Genetics|October 1, 1987
Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14A F Wright, S S Bhattacharya, J F Clayton, et al.Pageof 18