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Journal Abstract Search

159 related items for PubMed ID: 7847373

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  • 2. Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14.
    Edwards AO, Miedziak A, Vrabec T, Verhoeven J, Acott TS, Weleber RG, Donoso LA.
    Am J Ophthalmol; 1999 Apr; 127(4):426-35. PubMed ID: 10218695
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  • 3. A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1.
    Kaplan J, Gerber S, Larget-Piet D, Rozet JM, Dollfus H, Dufier JL, Odent S, Postel-Vinay A, Janin N, Briard ML.
    Nat Genet; 1993 Nov; 5(3):308-11. PubMed ID: 8275096
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  • 4. A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p.
    Anderson KL, Baird L, Lewis RA, Chinault AC, Otterud B, Leppert M, Lupski JR.
    Am J Hum Genet; 1995 Dec; 57(6):1351-63. PubMed ID: 8533764
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  • 10. A dominant Stargardt's macular dystrophy locus maps to chromosome 13q34.
    Zhang K, Bither PP, Park R, Donoso LA, Seidman JG, Seidman CE.
    Arch Ophthalmol; 1994 Jun; 112(6):759-64. PubMed ID: 8002833
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  • 11. An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5.
    Michaelides M, Johnson S, Tekriwal AK, Holder GE, Bellmann C, Kinning E, Woodruff G, Trembath RC, Hunt DM, Moore AT.
    Invest Ophthalmol Vis Sci; 2003 May; 44(5):2178-83. PubMed ID: 12714659
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  • 13. A new locus for autosomal recessive retinitis pigmentosa (RP19) maps to 1p13-1p21.
    Martínez-Mir A, Bayés M, Vilageliu L, Grinberg D, Ayuso C, del Río T, García-Sandoval B, Bussaglia E, Baiget M, Gonzàlez-Duarte R, Balcells S.
    Genomics; 1997 Feb 15; 40(1):142-6. PubMed ID: 9070931
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  • 15. Autosomal dominant macular dystrophy simulating North Carolina macular dystrophy.
    Holz FG, Evans K, Gregory CY, Bhattacharya S, Bird AC.
    Arch Ophthalmol; 1995 Feb 15; 113(2):178-84. PubMed ID: 7864750
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  • 16. Stargardt disease: linkage to the ABCR gene region on 1p21-p22 in Scandinavian families.
    Arnell H, Mäntyjärvi M, Tuppurainen K, Andréasson S, Dahl N.
    Acta Ophthalmol Scand; 1998 Dec 15; 76(6):649-52. PubMed ID: 9881544
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  • 17. Age-related macular degeneration. Clinical features in a large family and linkage to chromosome 1q.
    Klein ML, Schultz DW, Edwards A, Matise TC, Rust K, Berselli CB, Trzupek K, Weleber RG, Ott J, Wirtz MK, Acott TS.
    Arch Ophthalmol; 1998 Aug 15; 116(8):1082-8. PubMed ID: 9715689
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  • 19. Clinical spectrum of chromosome 6-linked autosomal dominant drusen and macular degeneration.
    Stefko ST, Zhang K, Gorin MB, Traboulsi EI.
    Am J Ophthalmol; 2000 Aug 15; 130(2):203-8. PubMed ID: 11004295
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  • 20. Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of cases.
    Weber BH, Sander S, Kopp C, Walker D, Eckstein A, Wissinger B, Zrenner E, Grimm T.
    Br J Ophthalmol; 1996 Aug 15; 80(8):745-9. PubMed ID: 8949721
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