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4. A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1. Michaelides M; Holder GE; Hunt DM; Fitzke FW; Bird AC; Moore AT Br J Ophthalmol; 2005 Feb; 89(2):198-206. PubMed ID: 15665353 [TBL] [Abstract][Full Text] [Related]
6. Progressive human cone-rod dysfunction (dystrophy). Fishman GA Trans Sect Ophthalmol Am Acad Ophthalmol Otolaryngol; 1976; 81(4 Pt 1):OP716-24. PubMed ID: 1085512 [TBL] [Abstract][Full Text] [Related]
7. Wide-field fundus autofluorescence abnormalities and visual function in patients with cone and cone-rod dystrophies. Oishi M; Oishi A; Ogino K; Makiyama Y; Gotoh N; Kurimoto M; Yoshimura N Invest Ophthalmol Vis Sci; 2014 May; 55(6):3572-7. PubMed ID: 24845635 [TBL] [Abstract][Full Text] [Related]
9. Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction. Roosing S; van den Born LI; Hoyng CB; Thiadens AA; de Baere E; Collin RW; Koenekoop RK; Leroy BP; van Moll-Ramirez N; Venselaar H; Riemslag FC; Cremers FP; Klaver CC; den Hollander AI Ophthalmology; 2013 Jun; 120(6):1239-46. PubMed ID: 23499059 [TBL] [Abstract][Full Text] [Related]
10. Young monozygotic twin sisters with fundus albipunctatus and cone dystrophy. Nakamura M; Lin J; Miyake Y Arch Ophthalmol; 2004 Aug; 122(8):1203-7. PubMed ID: 15302662 [TBL] [Abstract][Full Text] [Related]
11. Autosomal recessive bestrophinopathy: differential diagnosis and treatment options. Boon CJ; van den Born LI; Visser L; Keunen JE; Bergen AA; Booij JC; Riemslag FC; Florijn RJ; van Schooneveld MJ Ophthalmology; 2013 Apr; 120(4):809-20. PubMed ID: 23290749 [TBL] [Abstract][Full Text] [Related]
12. Mutation in the gene GUCA1A, encoding guanylate cyclase-activating protein 1, causes cone, cone-rod, and macular dystrophy. Michaelides M; Wilkie SE; Jenkins S; Holder GE; Hunt DM; Moore AT; Webster AR Ophthalmology; 2005 Aug; 112(8):1442-7. PubMed ID: 15953638 [TBL] [Abstract][Full Text] [Related]
14. Cone-rod retinal dystrophy in a patient with neurofibromatosis type 1. Kylstra JA; Aylsworth AS Can J Ophthalmol; 1993 Apr; 28(2):79-80. PubMed ID: 8508343 [No Abstract] [Full Text] [Related]
15. A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews. Auslender N; Sharon D; Abbasi AH; Garzozi HJ; Banin E; Ben-Yosef T Invest Ophthalmol Vis Sci; 2007 Dec; 48(12):5431-8. PubMed ID: 18055789 [TBL] [Abstract][Full Text] [Related]
16. A case of progressive cone dystrophy with marked asymmetry in the fundus. Yamaguchi K; Kinpara Y; Hara S Ann Ophthalmol; 1991 Apr; 23(4):145-7. PubMed ID: 2064257 [TBL] [Abstract][Full Text] [Related]
17. High-resolution retinal imaging of cone-rod dystrophy. Wolfing JI; Chung M; Carroll J; Roorda A; Williams DR Ophthalmology; 2006 Jun; 113(6):1019.e1. PubMed ID: 16650474 [TBL] [Abstract][Full Text] [Related]
18. X-linked cone dystrophy. An overlooked diagnosis? Pinckers A; Deutman AF Int Ophthalmol; 1987 Aug; 10(4):241-3. PubMed ID: 3498700 [TBL] [Abstract][Full Text] [Related]
19. Cone-rod dystrophy: a case report. Norden LC; Amos JF; Newcomb RD Am J Optom Physiol Opt; 1978 Dec; 55(12):824-35. PubMed ID: 313711 [TBL] [Abstract][Full Text] [Related]
20. Spectral-domain optical coherence tomography and fundus autofluorescence characteristics in patients with fundus albipunctatus and retinitis punctata albescens. Genead MA; Fishman GA; Lindeman M Ophthalmic Genet; 2010 Jun; 31(2):66-72. PubMed ID: 20450307 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]