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Human Mutation
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September 27, 2002
Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 gene
Michèle M Sale, Jamie E Craig, Jacinta C Charlesworth, et al.
American Journal of Human Genetics
|
February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye
D Y Nishimura, C C Searby, W L Alward, et al.
Investigative Ophthalmology & Visual Science
|
May 4, 2010
Genetic association of insulin-like growth factor-1 polymorphisms with high-grade myopia in an international family cohort
Ravikanth Metlapally, Chang-Seok Ki, Yi-Ju Li, et al.
Human Mutation
|
March 24, 2009
Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract
Tianxiao Zhang, Rui Hua, Wei Xiao, et al.
Molecular Vision
|
June 14, 2013
Interrogation of the platelet-derived growth factor receptor alpha locus and corneal astigmatism in Australians of Northern European ancestry: results of a genome-wide association study
Seyhan Yazar, Aniket Mishra, Wei Ang, et al.
Disability and Rehabilitation
|
November 14, 2008
Novel methods for tendon investigations
M Kjaer, H Langberg, J Bojsen-Møller, et al.
Clinical & Experimental Ophthalmology
|
October 14, 2014
Pterygium and conjunctival ultraviolet autofluorescence in young Australian adults: the Raine study
Charlotte M McKnight, Justin C Sherwin, Seyhan Yazar, et al.
American Journal of Ophthalmology
|
July 30, 2014
Myopia in young adults is inversely related to an objective marker of ocular sun exposure: the Western Australian Raine cohort study
Charlotte M McKnight, Justin C Sherwin, Seyhan Yazar, et al.
Clinical Ophthalmology (Auckland, N.Z.)
|
April 15, 2010
Primary open angle glaucoma due to T377M MYOC: Population mapping of a Greek founder mutation in Northwestern Greece
George Kitsos, Zacharias Petrou, Maria Grigoriadou, et al.
Scientific Reports
|
October 6, 2020
Deep learning segmentation of hyperautofluorescent fleck lesions in Stargardt disease
Jason Charng, Di Xiao, Maryam Mehdizadeh, et al.
Page
of 77
Search research articles
Search
Showing results (551-560 of 763) with videos related to
Sort By:
Page
of 77
Human Mutation
|
September 27, 2002
Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 gene
Michèle M Sale, Jamie E Craig, Jacinta C Charlesworth, et al.
American Journal of Human Genetics
|
February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye
D Y Nishimura, C C Searby, W L Alward, et al.
Investigative Ophthalmology & Visual Science
|
May 4, 2010
Genetic association of insulin-like growth factor-1 polymorphisms with high-grade myopia in an international family cohort
Ravikanth Metlapally, Chang-Seok Ki, Yi-Ju Li, et al.
Human Mutation
|
March 24, 2009
Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract
Tianxiao Zhang, Rui Hua, Wei Xiao, et al.
Molecular Vision
|
June 14, 2013
Interrogation of the platelet-derived growth factor receptor alpha locus and corneal astigmatism in Australians of Northern European ancestry: results of a genome-wide association study
Seyhan Yazar, Aniket Mishra, Wei Ang, et al.
Disability and Rehabilitation
|
November 14, 2008
Novel methods for tendon investigations
M Kjaer, H Langberg, J Bojsen-Møller, et al.
Clinical & Experimental Ophthalmology
|
October 14, 2014
Pterygium and conjunctival ultraviolet autofluorescence in young Australian adults: the Raine study
Charlotte M McKnight, Justin C Sherwin, Seyhan Yazar, et al.
American Journal of Ophthalmology
|
July 30, 2014
Myopia in young adults is inversely related to an objective marker of ocular sun exposure: the Western Australian Raine cohort study
Charlotte M McKnight, Justin C Sherwin, Seyhan Yazar, et al.
Clinical Ophthalmology (Auckland, N.Z.)
|
April 15, 2010
Primary open angle glaucoma due to T377M MYOC: Population mapping of a Greek founder mutation in Northwestern Greece
George Kitsos, Zacharias Petrou, Maria Grigoriadou, et al.
Scientific Reports
|
October 6, 2020
Deep learning segmentation of hyperautofluorescent fleck lesions in Stargardt disease
Jason Charng, Di Xiao, Maryam Mehdizadeh, et al.
Page
of 77