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American Journal of Ophthalmology
|
February 20, 2007
Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutations
Amy C Cohn, Carmel Toomes, Catherine Potter, et al.
Molecular Vision
|
April 3, 2010
Candidate gene study to investigate the genetic determinants of normal variation in central corneal thickness
David P Dimasi, Kathryn P Burdon, Alex W Hewitt, et al.
American Journal of Human Genetics
|
May 8, 2026
The impact of sex on the immune system explored at the single-cell level
Seyhan Yazar, Jose Alquicira-Hernandez, Kristof Wing, et al.
Optics Express
|
July 1, 2010
Automated volumetric evaluation of stereoscopic disc photography
Juan Xu, Hiroshi Ishikawa, Gadi Wollstein, et al.
Ophthalmology
|
December 4, 2010
Optic disc evaluation in optic neuropathies: the optic disc assessment project
Evelyn C O'Neill, Helen V Danesh-Meyer, George X Y Kong, et al.
ACS Synthetic Biology
|
October 11, 2022
The VEGAS Platform Is Unsuitable for Mammalian Directed Evolution
Christopher E Denes, Alexander J Cole, Minh Thuan Nguyen Tran, et al.
Experimental Eye Research
|
March 22, 2016
Biological effect of LOXL1 coding variants associated with pseudoexfoliation syndrome
Shiwani Sharma, Sarah Martin, Matthew J Sykes, et al.
Clinical & Experimental Ophthalmology
|
April 21, 2015
Clinical and molecular characterization of females affected by X-linked retinoschisis
Sandra E Staffieri, Loreto Rose, Andrew Chang, et al.
Scientific Reports
|
April 14, 2017
DNA methylation landscape of ocular tissue relative to matched peripheral blood
Alex W Hewitt, Vania Januar, Alexandra Sexton-Oates, et al.
Clinical & Experimental Ophthalmology
|
October 20, 2012
Establishment and evolution of the Australian Inherited Retinal Disease Register and DNA Bank
John N De Roach, Terri L McLaren, Rachel L Paterson, et al.
Page
of 43
Search research articles
Search
Showing results (151-160 of 425) with videos related to
Sort By:
Page
of 43
American Journal of Ophthalmology
|
February 20, 2007
Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutations
Amy C Cohn, Carmel Toomes, Catherine Potter, et al.
Molecular Vision
|
April 3, 2010
Candidate gene study to investigate the genetic determinants of normal variation in central corneal thickness
David P Dimasi, Kathryn P Burdon, Alex W Hewitt, et al.
American Journal of Human Genetics
|
May 8, 2026
The impact of sex on the immune system explored at the single-cell level
Seyhan Yazar, Jose Alquicira-Hernandez, Kristof Wing, et al.
Optics Express
|
July 1, 2010
Automated volumetric evaluation of stereoscopic disc photography
Juan Xu, Hiroshi Ishikawa, Gadi Wollstein, et al.
Ophthalmology
|
December 4, 2010
Optic disc evaluation in optic neuropathies: the optic disc assessment project
Evelyn C O'Neill, Helen V Danesh-Meyer, George X Y Kong, et al.
ACS Synthetic Biology
|
October 11, 2022
The VEGAS Platform Is Unsuitable for Mammalian Directed Evolution
Christopher E Denes, Alexander J Cole, Minh Thuan Nguyen Tran, et al.
Experimental Eye Research
|
March 22, 2016
Biological effect of LOXL1 coding variants associated with pseudoexfoliation syndrome
Shiwani Sharma, Sarah Martin, Matthew J Sykes, et al.
Clinical & Experimental Ophthalmology
|
April 21, 2015
Clinical and molecular characterization of females affected by X-linked retinoschisis
Sandra E Staffieri, Loreto Rose, Andrew Chang, et al.
Scientific Reports
|
April 14, 2017
DNA methylation landscape of ocular tissue relative to matched peripheral blood
Alex W Hewitt, Vania Januar, Alexandra Sexton-Oates, et al.
Clinical & Experimental Ophthalmology
|
October 20, 2012
Establishment and evolution of the Australian Inherited Retinal Disease Register and DNA Bank
John N De Roach, Terri L McLaren, Rachel L Paterson, et al.
Page
of 43