Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C Gail Summers

Showing results (61-70 of 75) with videos related to

Pageof 8
Sort By:
Human Genetics|September 19, 2003
Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotypeRichard A King, Jacy Pietsch, James P Fryer, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|March 16, 2010
Outcome of angle surgery in children with aphakic glaucomaErick D Bothun, Yan Guo, Stephen P Christiansen, et al.
Journal of Inherited Metabolic Disease|February 24, 2012
Clinical overview and treatment options for non-skeletal manifestations of mucopolysaccharidosis type IVAChristian J Hendriksz, Maisoon Al-Jawad, Kenneth I Berger, et al.
Investigative Ophthalmology & Visual Science|March 21, 2020
Assessing Ganglion Cell Layer Topography in Human Albinism Using Optical Coherence TomographyErica N Woertz, Bisola S Omoba, Taylor M Dunn, et al.
American Journal of Human Genetics|July 24, 2003
MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2)Richard A King, Rebecca K Willaert, Ramona M Schmidt, et al.
Journal of Pediatric Ophthalmology and Strabismus|June 9, 2015
Clinical Insights Into Foveal Morphology in AlbinismBrandon K McCafferty, Melissa A Wilk, John T McAllister, et al.
American Journal of Ophthalmology|August 20, 2013
A comparison of treatment approaches for bilateral congenital nasolacrimal duct obstructionKatherine A Lee, Danielle L Chandler, Michael X Repka, et al.
Investigative Ophthalmology & Visual Science|March 5, 2024
Quantitative Foveal Structural Metrics as Predictors of Visual Acuity in Human AlbinismErica N Woertz, Gelique D Ayala, Niamh Wynne, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2012
β-Blocking and racial variation in the severity of retinopathy of prematurityWilliam V Good, Robert J Hardy, David K Wallace, et al.
American Journal of Human Genetics|June 14, 2011
A BLOC-1 mutation screen reveals that PLDN is mutated in Hermansky-Pudlak Syndrome type 9Andrew R Cullinane, James A Curry, Carmelo Carmona-Rivera, et al.
Pageof 8

Showing results (61-70 of 75) with videos related to

Sort By:
Pageof 8
Human Genetics|September 19, 2003
Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotypeRichard A King, Jacy Pietsch, James P Fryer, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|March 16, 2010
Outcome of angle surgery in children with aphakic glaucomaErick D Bothun, Yan Guo, Stephen P Christiansen, et al.
Journal of Inherited Metabolic Disease|February 24, 2012
Clinical overview and treatment options for non-skeletal manifestations of mucopolysaccharidosis type IVAChristian J Hendriksz, Maisoon Al-Jawad, Kenneth I Berger, et al.
Investigative Ophthalmology & Visual Science|March 21, 2020
Assessing Ganglion Cell Layer Topography in Human Albinism Using Optical Coherence TomographyErica N Woertz, Bisola S Omoba, Taylor M Dunn, et al.
American Journal of Human Genetics|July 24, 2003
MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2)Richard A King, Rebecca K Willaert, Ramona M Schmidt, et al.
Journal of Pediatric Ophthalmology and Strabismus|June 9, 2015
Clinical Insights Into Foveal Morphology in AlbinismBrandon K McCafferty, Melissa A Wilk, John T McAllister, et al.
American Journal of Ophthalmology|August 20, 2013
A comparison of treatment approaches for bilateral congenital nasolacrimal duct obstructionKatherine A Lee, Danielle L Chandler, Michael X Repka, et al.
Investigative Ophthalmology & Visual Science|March 5, 2024
Quantitative Foveal Structural Metrics as Predictors of Visual Acuity in Human AlbinismErica N Woertz, Gelique D Ayala, Niamh Wynne, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2012
β-Blocking and racial variation in the severity of retinopathy of prematurityWilliam V Good, Robert J Hardy, David K Wallace, et al.
American Journal of Human Genetics|June 14, 2011
A BLOC-1 mutation screen reveals that PLDN is mutated in Hermansky-Pudlak Syndrome type 9Andrew R Cullinane, James A Curry, Carmelo Carmona-Rivera, et al.
Pageof 8