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Translational Vision Science & Technology
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February 22, 2018
Crowd-sourced Ontology for Photoleukocoria: Identifying Common Internet Search Terms for a Potentially Important Pediatric Ophthalmic Sign
Sandra E Staffieri, Lisa S Kearns, Paul G Sanfilippo, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
January 13, 2010
Association between erythropoietin gene polymorphisms and diabetic retinopathy
Scotoodeh Abhary, Sotoodeh Abhary, Kathryn P Burdon, et al.
Ophthalmic Genetics
|
April 25, 2007
No maternally inherited diabetes and deafness mutations in a sample of 193 Tasmanian diabetics with glaucoma
R C Andrew Symons, Rustamzhon Turakulov, Simon J Foote, et al.
BMC Medical Genetics
|
November 25, 2010
A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32
Kathryn Hattersley, Kate J Laurie, Jan E Liebelt, et al.
Plos One
|
March 9, 2010
Sequence variation in DDAH1 and DDAH2 genes is strongly and additively associated with serum ADMA concentrations in individuals with type 2 diabetes
Sotoodeh Abhary, Kathryn P Burdon, Abraham Kuot, et al.
Molecular Vision
|
November 9, 2019
Autosomal dominant nanophthalmos and high hyperopia associated with a C-terminal frameshift variant in <i>MYRF</i>
Owen M Siggs, Emmanuelle Souzeau, James Breen, et al.
Molecular Vision
|
April 24, 2008
A novel locus for X-linked congenital cataract on Xq24
Jamie E Craig, Kathryn L Friend, Jozef Gecz, et al.
BMC Medical Genetics
|
May 10, 2017
Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)
Shari Javadiyan, Jamie E Craig, Shiwani Sharma, et al.
Eye (London, England)
|
December 13, 2022
Cost-effectiveness of polygenic risk profiling for primary open-angle glaucoma in the United Kingdom and Australia
Qinqin Liu, John Davis, Xikun Han, et al.
Ophthalmic Genetics
|
March 23, 2002
Investigation of the prevalence of the myocilin Q368STOP mutation in Ugandan glaucoma patients
Michèle M Sale, Liesel M FitzGerald, Kenneth Kagame, et al.
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of 36
Search research articles
Search
Showing results (101-110 of 352) with videos related to
Sort By:
Page
of 36
Translational Vision Science & Technology
|
February 22, 2018
Crowd-sourced Ontology for Photoleukocoria: Identifying Common Internet Search Terms for a Potentially Important Pediatric Ophthalmic Sign
Sandra E Staffieri, Lisa S Kearns, Paul G Sanfilippo, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
January 13, 2010
Association between erythropoietin gene polymorphisms and diabetic retinopathy
Scotoodeh Abhary, Sotoodeh Abhary, Kathryn P Burdon, et al.
Ophthalmic Genetics
|
April 25, 2007
No maternally inherited diabetes and deafness mutations in a sample of 193 Tasmanian diabetics with glaucoma
R C Andrew Symons, Rustamzhon Turakulov, Simon J Foote, et al.
BMC Medical Genetics
|
November 25, 2010
A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32
Kathryn Hattersley, Kate J Laurie, Jan E Liebelt, et al.
Plos One
|
March 9, 2010
Sequence variation in DDAH1 and DDAH2 genes is strongly and additively associated with serum ADMA concentrations in individuals with type 2 diabetes
Sotoodeh Abhary, Kathryn P Burdon, Abraham Kuot, et al.
Molecular Vision
|
November 9, 2019
Autosomal dominant nanophthalmos and high hyperopia associated with a C-terminal frameshift variant in <i>MYRF</i>
Owen M Siggs, Emmanuelle Souzeau, James Breen, et al.
Molecular Vision
|
April 24, 2008
A novel locus for X-linked congenital cataract on Xq24
Jamie E Craig, Kathryn L Friend, Jozef Gecz, et al.
BMC Medical Genetics
|
May 10, 2017
Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)
Shari Javadiyan, Jamie E Craig, Shiwani Sharma, et al.
Eye (London, England)
|
December 13, 2022
Cost-effectiveness of polygenic risk profiling for primary open-angle glaucoma in the United Kingdom and Australia
Qinqin Liu, John Davis, Xikun Han, et al.
Ophthalmic Genetics
|
March 23, 2002
Investigation of the prevalence of the myocilin Q368STOP mutation in Ugandan glaucoma patients
Michèle M Sale, Liesel M FitzGerald, Kenneth Kagame, et al.
Page
of 36