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JAMA Ophthalmology
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August 11, 2022
Severe Familial Exudative Vitreoretinopathy, Congenital Hearing Loss, and Developmental Delay in a Child With Biallelic Variants in FZD4
Sarah R van der Ende, Benjamin S Meyers, Jenina E Capasso, et al.
The Journal of Clinical Investigation
|
December 5, 2017
Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach
Simon M Petersen-Jones, Laurence M Occelli, Paige A Winkler, et al.
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Search research articles
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Showing results (21-30 of 22) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 22 results.
JAMA Ophthalmology
|
August 11, 2022
Severe Familial Exudative Vitreoretinopathy, Congenital Hearing Loss, and Developmental Delay in a Child With Biallelic Variants in FZD4
Sarah R van der Ende, Benjamin S Meyers, Jenina E Capasso, et al.
The Journal of Clinical Investigation
|
December 5, 2017
Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach
Simon M Petersen-Jones, Laurence M Occelli, Paige A Winkler, et al.
Page
of 3