All Stories

  1. Next-generation sequencing targeted disease panel in rod-cone retinal dystrophies in Māori and Polynesian reveals novel changes and a common founder mutation
  2. Novel gene mutation in a patient with Bietti crystalline dystrophy without corneal deposits
  3. Macular disease genetics and supplementation: the evidence for choosing wisely
  4. Retinal haemorrhages in a child struck by a barbell
  5. What genetics has taught us about keratoconus
  6. Corneal dystrophies and genetics in the International Committee for Classification of Corneal Dystrophies era: a review
  7. Blepharophimosis and bilateral Duane syndrome associated with a FOXL2 mutation
  8. Prosthetic conformers: a step towards improved rehabilitation of enucleated children
  9. Digenic Inheritance of Early-Onset Glaucoma: CYP1B1, a Potential Modifier Gene