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D Ebenezer

Showing results (31-40 of 61) with videos related to

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Human Molecular Genetics|October 29, 2004
Recombination hotspots and block structure of linkage disequilibrium in the human genome exemplified by detailed analysis of PGM1 on 1p31Naheed A Rana, Neil D Ebenezer, Andrew R Webster, et al.
Journal of Medical Genetics|August 16, 2003
Prevalence of optineurin sequence variants in adult primary open angle glaucoma: implications for diagnostic testingT Aung, N D Ebenezer, G Brice, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 15, 2005
Clinical and molecular characterization of a family with autosomal recessive cornea planaNeil D Ebenezer, Chetankumar B Patel, Seenu M Hariprasad, 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.
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.
Histochemistry and Cell Biology|September 1, 2006
Differential immunogold localisation of sulphated and unsulphated keratan sulphate proteoglycans in normal and macular dystrophy cornea using sulphation motif-specific antibodiesRobert D Young, Tomoya O Akama, Petra Liskova, et al.
Ophthalmic Research|February 9, 2008
Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech familiesPetra Liskova, Gordon K Klintworth, Brandy L Bowling, et al.
Human Genetics|June 20, 2002
Investigating the association between OPA1 polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucomaTin Aung, Louise Ocaka, Neil D Ebenezer, 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.
Investigative Ophthalmology & Visual Science|November 24, 2005
Posterior polymorphous corneal dystrophy in Czech families maps to chromosome 20 and excludes the VSX1 geneRhian Gwilliam, Petra Liskova, Martin Filipec, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|October 29, 2004
Recombination hotspots and block structure of linkage disequilibrium in the human genome exemplified by detailed analysis of PGM1 on 1p31Naheed A Rana, Neil D Ebenezer, Andrew R Webster, et al.
Journal of Medical Genetics|August 16, 2003
Prevalence of optineurin sequence variants in adult primary open angle glaucoma: implications for diagnostic testingT Aung, N D Ebenezer, G Brice, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 15, 2005
Clinical and molecular characterization of a family with autosomal recessive cornea planaNeil D Ebenezer, Chetankumar B Patel, Seenu M Hariprasad, 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.
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.
Histochemistry and Cell Biology|September 1, 2006
Differential immunogold localisation of sulphated and unsulphated keratan sulphate proteoglycans in normal and macular dystrophy cornea using sulphation motif-specific antibodiesRobert D Young, Tomoya O Akama, Petra Liskova, et al.
Ophthalmic Research|February 9, 2008
Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech familiesPetra Liskova, Gordon K Klintworth, Brandy L Bowling, et al.
Human Genetics|June 20, 2002
Investigating the association between OPA1 polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucomaTin Aung, Louise Ocaka, Neil D Ebenezer, 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.
Investigative Ophthalmology & Visual Science|November 24, 2005
Posterior polymorphous corneal dystrophy in Czech families maps to chromosome 20 and excludes the VSX1 geneRhian Gwilliam, Petra Liskova, Martin Filipec, et al.
Pageof 7