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Jamie E Craig

Showing results (201-210 of 352) with videos related to

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Clinical & Experimental Ophthalmology|September 15, 2006
Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurityJoanne L Dickinson, Michèle M Sale, Abraham Passmore, et al.
Ophthalmology|December 21, 2016
Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk IndividualsEmmanuelle Souzeau, Kien Hou Tram, Martin Witney, et al.
Investigative Ophthalmology & Visual Science|September 28, 2005
Central corneal thickness is highly heritable: the twin eye studiesTze'Yo Toh, S H Melissa Liew, Jane R MacKinnon, et al.
European Journal of Human Genetics : EJHG|April 19, 2021
A 127 kb truncating deletion of PGRMC1 is a novel cause of X-linked isolated paediatric cataractJohanna L Jones, Mark A Corbett, Elise Yeaman, et al.
Molecular Vision|March 10, 2015
CYP1B1 copy number variation is not a major contributor to primary congenital glaucomaEmmanuelle Souzeau, Melanie Hayes, Jonathan B Ruddle, et al.
Molecular Genetics & Genomic Medicine|May 18, 2018
Identification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri LankaShari Javadiyan, Sionne E M Lucas, Dechen Wangmo, et al.
Human Mutation|September 27, 2002
Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 geneMichèle M Sale, Jamie E Craig, Jacinta C Charlesworth, et al.
Plos One|June 21, 2018
Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descentSionne E M Lucas, Tiger Zhou, Nicholas B Blackburn, et al.
Human Mutation|March 24, 2009
Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataractTianxiao Zhang, Rui Hua, Wei Xiao, et al.
Clinical & Experimental Ophthalmology|October 19, 2017
Visual outcomes following vitrectomy for diabetic retinopathy amongst Indigenous and non-Indigenous Australians in South Australia and the Northern TerritoryGeorgia Kaidonis, Mark M Hassall, Russell Phillips, et al.
Pageof 36

Showing results (201-210 of 352) with videos related to

Sort By:
Pageof 36
Clinical & Experimental Ophthalmology|September 15, 2006
Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurityJoanne L Dickinson, Michèle M Sale, Abraham Passmore, et al.
Ophthalmology|December 21, 2016
Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk IndividualsEmmanuelle Souzeau, Kien Hou Tram, Martin Witney, et al.
Investigative Ophthalmology & Visual Science|September 28, 2005
Central corneal thickness is highly heritable: the twin eye studiesTze'Yo Toh, S H Melissa Liew, Jane R MacKinnon, et al.
European Journal of Human Genetics : EJHG|April 19, 2021
A 127 kb truncating deletion of PGRMC1 is a novel cause of X-linked isolated paediatric cataractJohanna L Jones, Mark A Corbett, Elise Yeaman, et al.
Molecular Vision|March 10, 2015
CYP1B1 copy number variation is not a major contributor to primary congenital glaucomaEmmanuelle Souzeau, Melanie Hayes, Jonathan B Ruddle, et al.
Molecular Genetics & Genomic Medicine|May 18, 2018
Identification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri LankaShari Javadiyan, Sionne E M Lucas, Dechen Wangmo, et al.
Human Mutation|September 27, 2002
Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 geneMichèle M Sale, Jamie E Craig, Jacinta C Charlesworth, et al.
Plos One|June 21, 2018
Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descentSionne E M Lucas, Tiger Zhou, Nicholas B Blackburn, et al.
Human Mutation|March 24, 2009
Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataractTianxiao Zhang, Rui Hua, Wei Xiao, et al.
Clinical & Experimental Ophthalmology|October 19, 2017
Visual outcomes following vitrectomy for diabetic retinopathy amongst Indigenous and non-Indigenous Australians in South Australia and the Northern TerritoryGeorgia Kaidonis, Mark M Hassall, Russell Phillips, et al.
Pageof 36