Related Experiment Videos
Cone-rod retinal dystrophy in a patient with neurofibromatosis type 1
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome.
Cell death and differentiation·2016
New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome.
Cytogenetic and genome research·2006
A molecular approach to dominance in hypophosphatasia.
Human genetics·2001
Clinical aspects of defects in the determination of laterality.
American journal of medical genetics·2001
Patient-reported outcome measures in cataract surgery: a systematic review and meta-analysis of visual function and quality of life.
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie·2026
Posterior capsule rupture during cataract surgery: analysis of visual outcomes and associated risk factors.
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie·2026
Predictors of loss to follow-up in neovascular age-related macular degeneration.
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie·2026
Vision care access programs for communities facing barriers to care in Canada: a systematic review.
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie·2026
Clinical and MRI outcomes of teprotumumab in Japanese thyroid eye disease.
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie·2026
Applications of artificial intelligence in rural ophthalmology: a scoping review.
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie·2026