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2. [Genetic aspects in pigmentary retinopathy]. Preoteasa D. Oftalmologia; 1996; 40(2):137-44. PubMed ID: 8717081 [Abstract] [Full Text] [Related]
3. [Pigmentary retinopathy and Coats' vasculopathy]. Munteanu C. Oftalmologia; 1990; 34(2):135-42. PubMed ID: 2101044 [Abstract] [Full Text] [Related]
4. A gene for primary congenital glaucoma is not linked to the locus on chromosome 1q for autosomal dominant juvenile-onset open angle glaucoma. Anderson KL, Lewis RA, Bejjani BA, Baird L, Otterud B, Tomey KF, Astle WF, Dueker DK, Leppert M, Lupski JR. J Glaucoma; 1996 Dec; 5(6):416-21. PubMed ID: 8946299 [Abstract] [Full Text] [Related]
16. A novel IMPDH1 mutation (Arg231Pro) in a family with a severe form of autosomal dominant retinitis pigmentosa. Grover S, Fishman GA, Stone EM. Ophthalmology; 2004 Oct 24; 111(10):1910-6. PubMed ID: 15465556 [Abstract] [Full Text] [Related]