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Investigative Ophthalmology & Visual Science
|
December 21, 2010
Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibility
Kylee L Spencer, Lana M Olson, Nathalie Schnetz-Boutaud, et al.
Ophthalmology. Glaucoma
|
April 25, 2025
Prevalence of Myocilin Mutations in a Cohort of Patients with Juvenile Open-Angle Glaucoma from sub-Saharan Africa
Olusola Olawoye, Brian P Young, Angela W Nyunt, et al.
Journal of Medical Genetics
|
July 31, 2025
Biallelic loss-of-function variants in <i>C19orf44</i> lead to retinal degeneration
Hafiz Muhammad Jafar Hussain, Wang Meng, Yumei Li, et al.
American Journal of Human Genetics
|
November 1, 1996
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients
M D Weston, P M Kelley, L D Overbeck, et al.
Frontiers in Neural Circuits
|
August 26, 2016
Peripheral Sensory Neurons Expressing Melanopsin Respond to Light
Anna Matynia, Eileen Nguyen, Xiaoping Sun, et al.
American Journal of Ophthalmology
|
April 29, 1998
Long-term tamoxifen citrate use and potential ocular toxicity
M B Gorin, R Day, J P Costantino, et al.
Human Molecular Genetics
|
May 24, 2012
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)
Tom R Webb, David A Parfitt, Jessica C Gardner, et al.
American Journal of Human Genetics
|
November 4, 2000
Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I
L M Astuto, M D Weston, C A Carney, et al.
American Journal of Human Genetics
|
May 29, 2004
Age-related maculopathy: a genomewide scan with continued evidence of susceptibility loci within the 1q31, 10q26, and 17q25 regions
Daniel E Weeks, Yvette P Conley, Hui-Ju Tsai, et al.
Experimental Eye Research
|
February 21, 2025
Dissecting the biological complexity of age-related macular degeneration: Is it one disease, multiple separate diseases, or a spectrum?
Jason M L Miller, Benjamin R Thompson, James T Handa, et al.
Page
of 18
Search research articles
Search
Showing results (141-150 of 175) with videos related to
Sort By:
Page
of 18
Investigative Ophthalmology & Visual Science
|
December 21, 2010
Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibility
Kylee L Spencer, Lana M Olson, Nathalie Schnetz-Boutaud, et al.
Ophthalmology. Glaucoma
|
April 25, 2025
Prevalence of Myocilin Mutations in a Cohort of Patients with Juvenile Open-Angle Glaucoma from sub-Saharan Africa
Olusola Olawoye, Brian P Young, Angela W Nyunt, et al.
Journal of Medical Genetics
|
July 31, 2025
Biallelic loss-of-function variants in <i>C19orf44</i> lead to retinal degeneration
Hafiz Muhammad Jafar Hussain, Wang Meng, Yumei Li, et al.
American Journal of Human Genetics
|
November 1, 1996
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients
M D Weston, P M Kelley, L D Overbeck, et al.
Frontiers in Neural Circuits
|
August 26, 2016
Peripheral Sensory Neurons Expressing Melanopsin Respond to Light
Anna Matynia, Eileen Nguyen, Xiaoping Sun, et al.
American Journal of Ophthalmology
|
April 29, 1998
Long-term tamoxifen citrate use and potential ocular toxicity
M B Gorin, R Day, J P Costantino, et al.
Human Molecular Genetics
|
May 24, 2012
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)
Tom R Webb, David A Parfitt, Jessica C Gardner, et al.
American Journal of Human Genetics
|
November 4, 2000
Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I
L M Astuto, M D Weston, C A Carney, et al.
American Journal of Human Genetics
|
May 29, 2004
Age-related maculopathy: a genomewide scan with continued evidence of susceptibility loci within the 1q31, 10q26, and 17q25 regions
Daniel E Weeks, Yvette P Conley, Hui-Ju Tsai, et al.
Experimental Eye Research
|
February 21, 2025
Dissecting the biological complexity of age-related macular degeneration: Is it one disease, multiple separate diseases, or a spectrum?
Jason M L Miller, Benjamin R Thompson, James T Handa, et al.
Page
of 18