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American Journal of Ophthalmology|November 16, 2023
Lisch Epithelial Corneal Dystrophy Is Caused by Heterozygous Loss-of-Function Variants in MCOLN1Karynne Patterson, Jessica X Chong, Doug D Chung, et al.
JAMA Ophthalmology|March 13, 2025
Genetic and Demographic Determinants of Fuchs Endothelial Corneal Dystrophy Risk and SeveritySiyin Liu, Amanda N Sadan, Nihar Bhattacharyya, et al.
Frontiers in Oncology|July 19, 2019
A Novel Translational Ovine Pulmonary Adenocarcinoma Model for Human Lung CancerMark E Gray, Paul Sullivan, Jamie R K Marland, et al.
Frontiers in Oncology|May 21, 2019
Ovine Pulmonary Adenocarcinoma: A Unique Model to Improve Lung Cancer ResearchMark E Gray, James Meehan, Paul Sullivan, et al.
American Journal of Human Genetics|January 31, 2012
X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment developmentTom R Webb, Mar Matarin, Jessica C Gardner, et al.
American Journal of Human Genetics|January 11, 2016
Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2Alice E Davidson, Petra Liskova, Cerys J Evans, et al.
Journal of Hand and Microsurgery|October 27, 2025
The shield multicentre collaborative: A study of hand surgeons' intraoperative radiation exposure and techniques to limit dosingIulia Marinescu, Cian M Hehir, Ferdia Browne, et al.
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