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27. Identification of novel locus for autosomal dominant butterfly shaped macular dystrophy on 5q21.2-q33.2. den Hollander AI; van Lith-Verhoeven JJ; Kersten FF; Heister JG; de Kovel CG; Deutman AF; Hoyng CB; Cremers FP J Med Genet; 2004 Sep; 41(9):699-702. PubMed ID: 15342701 [No Abstract] [Full Text] [Related]
28. North Carolina macular dystrophy: clinical features, genealogy, and genetic linkage analysis. Small KW Trans Am Ophthalmol Soc; 1998; 96():925-61. PubMed ID: 10360311 [TBL] [Abstract][Full Text] [Related]
29. New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report. Blanco-Kelly F; Rodrigues-Jacy da Silva L; Sanchez-Navarro I; Riveiro-Alvarez R; Lopez-Martinez MA; Corton M; Ayuso C BMC Med Genet; 2017 Jan; 18(1):1. PubMed ID: 28061825 [TBL] [Abstract][Full Text] [Related]
30. Exclusion of TIMP3 as a candidate locus in age-related macular degeneration. De La Paz MA; Pericak-Vance MA; Lennon F; Haines JL; Seddon JM Invest Ophthalmol Vis Sci; 1997 May; 38(6):1060-5. PubMed ID: 9152225 [TBL] [Abstract][Full Text] [Related]
31. Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33-q27.3. John P; Ali G; Chishti MS; Naqvi SM; Leal SM; Ahmad W Hum Genet; 2006 Jan; 118(5):665-7. PubMed ID: 16273389 [TBL] [Abstract][Full Text] [Related]
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33. [Heredity in Stargardt disease and fundus flavimaculatus]. Turut P; Puech B Ophtalmologie; 1989; 3(3):187-92. PubMed ID: 2641107 [TBL] [Abstract][Full Text] [Related]
34. A homozygous frameshift mutation in BEST1 causes the classical form of Best disease in an autosomal recessive mode. Bitner H; Mizrahi-Meissonnier L; Griefner G; Erdinest I; Sharon D; Banin E Invest Ophthalmol Vis Sci; 2011 Jul; 52(8):5332-8. PubMed ID: 21467170 [TBL] [Abstract][Full Text] [Related]
35. [From gene to disease: from the ABCA4 gene to Stargardt disease, cone-rod dystrophy and retinitis pigmentosa]. Cremers FP; Maugeri A; Klevering BJ; Hoefsloot LH; Hoyng CB Ned Tijdschr Geneeskd; 2002 Aug; 146(34):1581-4. PubMed ID: 12224481 [TBL] [Abstract][Full Text] [Related]
36. [Stargardt's disease--ocular findings and family studies in Finnish patients]. Mäntyjärvi M; Tuppurainen K Duodecim; 1992; 108(14):1253-60. PubMed ID: 1366081 [No Abstract] [Full Text] [Related]
37. Vitelliform macular dystrophy of late onset. Wiznia RA; Perina B; Noble KG Br J Ophthalmol; 1981 Dec; 65(12):866-8. PubMed ID: 7317335 [TBL] [Abstract][Full Text] [Related]
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39. Abnormalities of visual-evoked potentials and pupillary light reflexes in a family with autosomal dominant occult macular dystrophy. Okuno T; Oku H; Kondo M; Miyake Y; Sugasawa J; Utsumi T; Ikeda T Clin Exp Ophthalmol; 2007 Nov; 35(8):781-3. PubMed ID: 17997791 [TBL] [Abstract][Full Text] [Related]