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Adam P DeLuca

Showing results (21-30 of 41) with videos related to

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Ophthalmology|June 1, 2017
Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal DiseaseEdwin M Stone, Jeaneen L Andorf, S Scott Whitmore, et al.
Human Molecular Genetics|November 6, 2023
Demonstration of the pathogenicity of a common non-exomic mutation in ABCA4 using iPSC-derived retinal organoids and retrospective clinical dataErin R Burnight, Beau J Fenner, Ian C Han, et al.
Scientific Reports|July 30, 2016
cGMP production of patient-specific iPSCs and photoreceptor precursor cells to treat retinal degenerative blindnessLuke A Wiley, Erin R Burnight, Adam P DeLuca, et al.
Ophthalmology. Retina|April 25, 2019
Wide-Field Swept-Source OCT and Angiography in X-Linked RetinoschisisIan C Han, S Scott Whitmore, D Brice Critser, et al.
Ophthalmology Science|November 29, 2023
Using Goldmann Visual Field Volume to Track Disease Progression in ChoroideremiaAdam P DeLuca, S Scott Whitmore, Nicole J Tatro, et al.
Retinal Cases & Brief Reports|November 26, 2019
AUTOIMMUNE RETINOPATHY MIMICKING HERITABLE RETINAL DEGENERATION IN A PATIENT WITH COMMON VARIABLE IMMUNE DEFICIENCYLuke A Wiley, Elaine M Binkley, Adam P DeLuca, et al.
Experimental Eye Research|March 19, 2013
Exon-level expression profiling of ocular tissuesAlex H Wagner, V Nikhil Anand, Wan-Heng Wang, et al.
Bioinformatics (Oxford, England)|August 16, 2014
Cordova: web-based management of genetic variation dataSean S Ephraim, Nikhil Anand, Adam P DeLuca, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 4, 2011
Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4)Jing Zheng, Katharine K Miller, Tao Yang, et al.
Human Mutation|January 3, 2013
AudioGene: predicting hearing loss genotypes from phenotypes to guide genetic screeningKyle R Taylor, Adam P Deluca, A Eliot Shearer, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Ophthalmology|June 1, 2017
Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal DiseaseEdwin M Stone, Jeaneen L Andorf, S Scott Whitmore, et al.
Human Molecular Genetics|November 6, 2023
Demonstration of the pathogenicity of a common non-exomic mutation in ABCA4 using iPSC-derived retinal organoids and retrospective clinical dataErin R Burnight, Beau J Fenner, Ian C Han, et al.
Scientific Reports|July 30, 2016
cGMP production of patient-specific iPSCs and photoreceptor precursor cells to treat retinal degenerative blindnessLuke A Wiley, Erin R Burnight, Adam P DeLuca, et al.
Ophthalmology. Retina|April 25, 2019
Wide-Field Swept-Source OCT and Angiography in X-Linked RetinoschisisIan C Han, S Scott Whitmore, D Brice Critser, et al.
Ophthalmology Science|November 29, 2023
Using Goldmann Visual Field Volume to Track Disease Progression in ChoroideremiaAdam P DeLuca, S Scott Whitmore, Nicole J Tatro, et al.
Retinal Cases & Brief Reports|November 26, 2019
AUTOIMMUNE RETINOPATHY MIMICKING HERITABLE RETINAL DEGENERATION IN A PATIENT WITH COMMON VARIABLE IMMUNE DEFICIENCYLuke A Wiley, Elaine M Binkley, Adam P DeLuca, et al.
Experimental Eye Research|March 19, 2013
Exon-level expression profiling of ocular tissuesAlex H Wagner, V Nikhil Anand, Wan-Heng Wang, et al.
Bioinformatics (Oxford, England)|August 16, 2014
Cordova: web-based management of genetic variation dataSean S Ephraim, Nikhil Anand, Adam P DeLuca, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 4, 2011
Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4)Jing Zheng, Katharine K Miller, Tao Yang, et al.
Human Mutation|January 3, 2013
AudioGene: predicting hearing loss genotypes from phenotypes to guide genetic screeningKyle R Taylor, Adam P Deluca, A Eliot Shearer, et al.
Pageof 5