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Journal Abstract Search

227 related items for PubMed ID: 9418727

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  • 24. Five novel RPGR mutations in families with X-linked retinitis pigmentosa.
    Guevara-Fujita M, Fahrner S, Buraczynska K, Cook J, Wheaton D, Cortes F, Vicencio C, Pena M, Fishman G, Mintz-Hittner H, Birch D, Hoffman D, Mears A, Fujita R, Swaroop A.
    Hum Mutat; 2001 Feb; 17(2):151. PubMed ID: 11180598
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  • 28. Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred.
    Wright AF, Bhattacharya SS, Aldred MA, Jay M, Carothers AD, Thomas NS, Bird AC, Jay B, Evans HJ.
    J Med Genet; 1991 Jul; 28(7):453-7. PubMed ID: 1895315
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  • 31. Positional cloning of the gene for X-linked retinitis pigmentosa 2.
    Schwahn U, Lenzner S, Dong J, Feil S, Hinzmann B, van Duijnhoven G, Kirschner R, Hemberger M, Bergen AA, Rosenberg T, Pinckers AJ, Fundele R, Rosenthal A, Cremers FP, Ropers HH, Berger W.
    Nat Genet; 1998 Aug; 19(4):327-32. PubMed ID: 9697692
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  • 33. A population-based epidemiological and genetic study of X-linked retinitis pigmentosa.
    Prokisch H, Hartig M, Hellinger R, Meitinger T, Rosenberg T.
    Invest Ophthalmol Vis Sci; 2007 Sep; 48(9):4012-8. PubMed ID: 17724181
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  • 36. Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa.
    Coleman M, Bhattacharya S, Lindsay S, Wright A, Jay M, Litt M, Craig I, Davies K.
    Am J Hum Genet; 1990 Dec; 47(6):935-40. PubMed ID: 2239970
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  • 37. Three novel mutations causing a truncated protein within the RP2 gene in Italian families with X-linked retinitis pigmentosa.
    De Luca A, Torrente I, Mangino M, Danesi R, Dallapiccola B, Novelli G.
    Mutat Res; 2001 Jan; 432(3-4):79-82. PubMed ID: 11465545
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  • 40. Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype.
    Ponjavic V, Andréasson S, Abrahamson M, Ehinger B, Gieser L, Fujita R, Swaroop A.
    Ophthalmic Genet; 1998 Dec; 19(4):187-96. PubMed ID: 9895243
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