These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. Selective loss of 11-cis vitamin A in an eye with hereditary chorioretinal degeneration similar to sector retinitis pigmentosa. Bridges CD; Alvarez RA Retina; 1982; 2(4):256-60. PubMed ID: 6101132 [No Abstract] [Full Text] [Related]
13. Persistence of fetal vasculature in a patient with Knobloch syndrome: potential role for endostatin in fetal vascular remodeling of the eye. Duh EJ; Yao YG; Dagli M; Goldberg MF Ophthalmology; 2004 Oct; 111(10):1885-8. PubMed ID: 15465551 [TBL] [Abstract][Full Text] [Related]
14. Molecular genetics of infantile-onset retinal dystrophies. Moradi P; Moore AT Eye (Lond); 2007 Oct; 21(10):1344-51. PubMed ID: 17914438 [TBL] [Abstract][Full Text] [Related]
15. [Developmental stages in hereditary juvenile macular degeneration]. François P; Turut P; Constantinides G Ber Zusammenkunft Dtsch Ophthalmol Ges; 1975; (73):217-23. PubMed ID: 1242920 [No Abstract] [Full Text] [Related]