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Journal Abstract Search

326 related items for PubMed ID: 9700209

  • 21. Assessment of mutations in the Best macular dystrophy (VMD2) gene in patients with adult-onset foveomacular vitelliform dystrophy, age-related maculopathy, and bull's-eye maculopathy.
    Seddon JM, Afshari MA, Sharma S, Bernstein PS, Chong S, Hutchinson A, Petrukhin K, Allikmets R.
    Ophthalmology; 2001 Nov; 108(11):2060-7. PubMed ID: 11713080
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  • 24. New gene found for inherited macular degeneration.
    Pennisi E.
    Science; 1998 Jul 03; 281(5373):31. PubMed ID: 9679014
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  • 26. A novel mutation of the VMD2 gene in a Chinese family with best vitelliform macular dystrophy.
    Li Y, Wang G, Dong B, Sun X, Turner MJ, Kamaya S, Zhang K.
    Ann Acad Med Singap; 2006 Jun 03; 35(6):408-10. PubMed ID: 16865191
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  • 29. New VMD2 gene mutations identified in patients affected by Best vitelliform macular dystrophy.
    Marchant D, Yu K, Bigot K, Roche O, Germain A, Bonneau D, Drouin-Garraud V, Schorderet DF, Munier F, Schmidt D, Le Neindre P, Marsac C, Menasche M, Dufier JL, Fischmeister R, Hartzell C, Abitbol M.
    J Med Genet; 2007 Mar 03; 44(3):e70. PubMed ID: 17287362
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  • 30. Bestrophins and retinopathies.
    Xiao Q, Hartzell HC, Yu K.
    Pflugers Arch; 2010 Jul 03; 460(2):559-69. PubMed ID: 20349192
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  • 31. Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM1.
    Nichols BE, Bascom R, Litt M, McInnes R, Sheffield VC, Stone EM.
    Am J Hum Genet; 1994 Jan 03; 54(1):95-103. PubMed ID: 8279475
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  • 32. Missense mutations in a retinal pigment epithelium protein, bestrophin-1, cause retinitis pigmentosa.
    Davidson AE, Millar ID, Urquhart JE, Burgess-Mullan R, Shweikh Y, Parry N, O'Sullivan J, Maher GJ, McKibbin M, Downes SM, Lotery AJ, Jacobson SG, Brown PD, Black GC, Manson FD.
    Am J Hum Genet; 2009 Nov 03; 85(5):581-92. PubMed ID: 19853238
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  • 35. Linkage studies of Best's macular dystrophy.
    Yoder FE, Cross HE, Chase GA, Fine SL, Freidhoff L, Machan CH, Bias WB.
    Clin Genet; 1988 Jul 03; 34(1):26-30. PubMed ID: 3165727
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  • 39. Genomic organization and mutation analysis of the gene encoding lecithin retinol acyltransferase in human retinal pigment epithelium.
    Ruiz A, Kuehn MH, Andorf JL, Stone E, Hageman GS, Bok D.
    Invest Ophthalmol Vis Sci; 2001 Jan 03; 42(1):31-7. PubMed ID: 11133845
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