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European Journal of Ophthalmology|September 15, 2020
A mutation in <i>CRX</i> causing pigmented paravenous retinochoroidal atrophyJin Kyun Oh, Yan Nuzbrokh, Winston Lee, et al.
Analytical Chemistry|August 3, 2017
Isothermal Point Mutation Detection: Toward a First-Pass Screening Strategy for Multidrug-Resistant TuberculosisBenjamin Y C Ng, Eugene J H Wee, Kyra Woods, et al.
Retinal Cases & Brief Reports|July 18, 2018
CHORIORETINAL CHANGES IN A GENETICALLY CONFIRMED CASE OF BOUCHER-NEUHÄUSER SYNDROMEBrittany B DeNaro, Elona Dhrami-Gavazi, David M Rubaltelli, et al.
Investigative Ophthalmology & Visual Science|October 13, 2020
Retinal Manifestations of Mitochondrial Oxidative Phosphorylation DisordersJin Kyun Oh, Jose Ronaldo Lima de Carvalho, Yan Nuzbrokh, et al.
Molecular Genetics & Genomic Medicine|May 27, 2017
Structural modeling of a novel <i>SLC38A8</i> mutation that causes foveal hypoplasiaMarcus A Toral, Gabriel Velez, Katherine Boudreault, et al.
Molecular Metabolism|June 6, 2017
Hepatic gene therapy rescues high-fat diet responses in circadian <i>Clock</i> mutant miceJudit Meyer-Kovac, Isa Kolbe, Lea Ehrhardt, et al.
Stem Cell Reports|March 12, 2020
MERTK-Dependent Ensheathment of Photoreceptor Outer Segments by Human Pluripotent Stem Cell-Derived Retinal Pigment EpitheliumSeba Almedawar, Katerina Vafia, Sven Schreiter, et al.
Cold Spring Harbor Molecular Case Studies|June 1, 2018
Extremely hypomorphic and severe deep intronic variants in the <i>ABCA4</i> locus result in varying Stargardt disease phenotypesJana Zernant, Winston Lee, Takayuki Nagasaki, et al.
International Journal of Psychiatry in Clinical Practice|January 6, 2012
Sino-American employer perspective about behavioral-driven health conditions: predictive analysesHector W H Tsang, Patrick W Corrigan, Kelvin M T Fung, et al.
The British Journal of Ophthalmology|May 12, 2009
Cellular origin of fundus autofluorescence in patients and mice with a defective NR2E3 geneN-K Wang, H F Fine, S Chang, et al.
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