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Human Genome Variation
|
October 28, 2020
Expanding the genetic spectrum of choroideremia in an Australian cohort: report of five novel <i>CHM</i> variants
Terri L McLaren, John N De Roach, Jennifer A Thompson, et al.
Human Molecular Genetics
|
November 13, 2024
Developing and validating a comprehensive polygenic risk score to enhance keratoconus risk prediction
Weixiong He, Urmo Võsa, Teele Palumaa, et al.
Journal of Glaucoma
|
June 5, 2003
Tonography demonstrates reduced facility of outflow of aqueous humor in myocilin mutation carriers
Colleen H Wilkinson, David van der Straaten, Jamie E Craig, et al.
Molecular Vision
|
December 20, 2008
Evaluation of splicing efficiency in lymphoblastoid cell lines from patients with splicing-factor retinitis pigmentosa
Lenka Ivings, Katherine V Towns, M A Matin, et al.
Journal of Glaucoma
|
April 15, 2020
Do Levels of Stress Markers Influence the Retinal Nerve Fiber Layer Thickness in Young Adults?
Samantha Sze-Yee Lee, Paul G Sanfilippo, Seyhan Yazar, et al.
Investigative Ophthalmology & Visual Science
|
December 23, 2020
Associations Between Fetal Growth Trajectories and the Development of Myopia by 20 Years of Age
Kathleen I C Dyer, Paul G Sanfilippo, Scott W White, et al.
Ophthalmology. Glaucoma
|
November 14, 2021
Attitudes Towards Polygenic Risk Testing in Individuals with Glaucoma
Georgina L Hollitt, Owen M Siggs, Bronwyn Ridge, et al.
Journal of Glaucoma
|
May 19, 2021
Physical Activity and Cardiovascular Fitness During Childhood and Adolescence: Association With Retinal Nerve Fibre Layer Thickness in Young Adulthood
Samantha Sze-Yee Lee, Joanne McVeigh, Leon Straker, et al.
Investigative Ophthalmology & Visual Science
|
May 28, 2010
Automated quantification of inherited phenotypes from color images: a twin study of the variability of optic nerve head shape
Li Tang, Todd E Scheetz, David A Mackey, et al.
Plos One
|
September 10, 2013
Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern Australia
Alpana Dave, Kate Laurie, Sandra E Staffieri, et al.
Page
of 50
Search research articles
Search
Showing results (231-240 of 499) with videos related to
Sort By:
Page
of 50
Human Genome Variation
|
October 28, 2020
Expanding the genetic spectrum of choroideremia in an Australian cohort: report of five novel <i>CHM</i> variants
Terri L McLaren, John N De Roach, Jennifer A Thompson, et al.
Human Molecular Genetics
|
November 13, 2024
Developing and validating a comprehensive polygenic risk score to enhance keratoconus risk prediction
Weixiong He, Urmo Võsa, Teele Palumaa, et al.
Journal of Glaucoma
|
June 5, 2003
Tonography demonstrates reduced facility of outflow of aqueous humor in myocilin mutation carriers
Colleen H Wilkinson, David van der Straaten, Jamie E Craig, et al.
Molecular Vision
|
December 20, 2008
Evaluation of splicing efficiency in lymphoblastoid cell lines from patients with splicing-factor retinitis pigmentosa
Lenka Ivings, Katherine V Towns, M A Matin, et al.
Journal of Glaucoma
|
April 15, 2020
Do Levels of Stress Markers Influence the Retinal Nerve Fiber Layer Thickness in Young Adults?
Samantha Sze-Yee Lee, Paul G Sanfilippo, Seyhan Yazar, et al.
Investigative Ophthalmology & Visual Science
|
December 23, 2020
Associations Between Fetal Growth Trajectories and the Development of Myopia by 20 Years of Age
Kathleen I C Dyer, Paul G Sanfilippo, Scott W White, et al.
Ophthalmology. Glaucoma
|
November 14, 2021
Attitudes Towards Polygenic Risk Testing in Individuals with Glaucoma
Georgina L Hollitt, Owen M Siggs, Bronwyn Ridge, et al.
Journal of Glaucoma
|
May 19, 2021
Physical Activity and Cardiovascular Fitness During Childhood and Adolescence: Association With Retinal Nerve Fibre Layer Thickness in Young Adulthood
Samantha Sze-Yee Lee, Joanne McVeigh, Leon Straker, et al.
Investigative Ophthalmology & Visual Science
|
May 28, 2010
Automated quantification of inherited phenotypes from color images: a twin study of the variability of optic nerve head shape
Li Tang, Todd E Scheetz, David A Mackey, et al.
Plos One
|
September 10, 2013
Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern Australia
Alpana Dave, Kate Laurie, Sandra E Staffieri, et al.
Page
of 50