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D Ebenezer

Showing results (41-50 of 61) with videos related to

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Molecular Vision|October 26, 2007
Molecular analysis of the VSX1 gene in familial keratoconusPetra Liskova, Neil D Ebenezer, Pirro G Hysi, et al.
The British Journal of Ophthalmology|June 19, 2003
A clinical, histopathological, and genetic study of Avellino corneal dystrophy in British familiesM F El-Ashry, M M Abd El-Aziz, D F P Larkin, et al.
Journal of Medical Genetics|October 13, 2007
Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtelL Ocaka, C Zhao, J A Reed, et al.
Plos One|October 11, 2012
High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutationPetra Liskova, Rhian Gwilliam, Martin Filipec, et al.
American Journal of Ophthalmology|January 18, 2005
Novel CHST6 nonsense and missense mutations responsible for macular corneal dystrophyMohamed F El-Ashry, Mai M Abd El-Aziz, Osama Shalaby, et al.
Investigative Ophthalmology & Visual Science|December 1, 2001
A novel keratocan mutation causing autosomal recessive cornea planaO J Lehmann, M F El-ashry, N D Ebenezer, et al.
American Journal of Human Genetics|September 29, 2000
Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucomaO J Lehmann, N D Ebenezer, T Jordan, et al.
The British Journal of Ophthalmology|March 20, 2004
An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 geneS S Dandekar, N D Ebenezer, C Grayson, et al.
Journal of Family Medicine and Primary Care|October 3, 2025
Anticoagulation in pregnant women with mechanical heart valves: A case series from a single centre in South India over two decadesArpudh Michael Anandaraj, Emily D Ebenezer, Annie P Vijjeswarapu, et al.
Journal of Medical Genetics|August 16, 2003
RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infectionsI Zito, S M Downes, R J Patel, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Molecular Vision|October 26, 2007
Molecular analysis of the VSX1 gene in familial keratoconusPetra Liskova, Neil D Ebenezer, Pirro G Hysi, et al.
The British Journal of Ophthalmology|June 19, 2003
A clinical, histopathological, and genetic study of Avellino corneal dystrophy in British familiesM F El-Ashry, M M Abd El-Aziz, D F P Larkin, et al.
Journal of Medical Genetics|October 13, 2007
Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtelL Ocaka, C Zhao, J A Reed, et al.
Plos One|October 11, 2012
High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutationPetra Liskova, Rhian Gwilliam, Martin Filipec, et al.
American Journal of Ophthalmology|January 18, 2005
Novel CHST6 nonsense and missense mutations responsible for macular corneal dystrophyMohamed F El-Ashry, Mai M Abd El-Aziz, Osama Shalaby, et al.
Investigative Ophthalmology & Visual Science|December 1, 2001
A novel keratocan mutation causing autosomal recessive cornea planaO J Lehmann, M F El-ashry, N D Ebenezer, et al.
American Journal of Human Genetics|September 29, 2000
Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucomaO J Lehmann, N D Ebenezer, T Jordan, et al.
The British Journal of Ophthalmology|March 20, 2004
An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 geneS S Dandekar, N D Ebenezer, C Grayson, et al.
Journal of Family Medicine and Primary Care|October 3, 2025
Anticoagulation in pregnant women with mechanical heart valves: A case series from a single centre in South India over two decadesArpudh Michael Anandaraj, Emily D Ebenezer, Annie P Vijjeswarapu, et al.
Journal of Medical Genetics|August 16, 2003
RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infectionsI Zito, S M Downes, R J Patel, et al.
Pageof 7