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Journal Abstract Search

146 related items for PubMed ID: 9443860

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  • 2. Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal Xp.
    Hardcastle AJ, David-Gray ZK, Jay M, Bird AC, Bhattacharya SS.
    Invest Ophthalmol Vis Sci; 1997 Dec; 38(13):2750-5. PubMed ID: 9418727
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  • 3. A new genetic locus for X linked progressive cone-rod dystrophy.
    Jalkanen R, Demirci FY, Tyynismaa H, Bech-Hansen T, Meindl A, Peippo M, Mäntyjärvi M, Gorin MB, Alitalo T.
    J Med Genet; 2003 Jun; 40(6):418-23. PubMed ID: 12807962
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  • 4. X-linked cone-rod dystrophy (locus COD1): identification of mutations in RPGR exon ORF15.
    Demirci FY, Rigatti BW, Wen G, Radak AL, Mah TS, Baic CL, Traboulsi EI, Alitalo T, Ramser J, Gorin MB.
    Am J Hum Genet; 2002 Apr; 70(4):1049-53. PubMed ID: 11857109
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  • 7. A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3.
    Fujita R, Bingham E, Forsythe P, McHenry C, Aita V, Navia BA, Dry K, Segal M, Devoto M, Bruns G, Wright AF, Ott J, Sieving PA, Swaroop A.
    Am J Hum Genet; 1996 Jul; 59(1):152-8. PubMed ID: 8659520
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  • 10. Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus.
    Zito I, Thiselton DL, Gorin MB, Stout JT, Plant C, Bird AC, Bhattacharya SS, Hardcastle AJ.
    Hum Genet; 1999 Jul; 105(1-2):57-62. PubMed ID: 10480356
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  • 13. Novel deletion of the RPGR gene in a Chinese family with X-linked retinitis pigmentosa.
    Zhao K, Wang L, Wang L, Wang L, Zhang Q, Wang Q.
    Ophthalmic Genet; 2001 Sep; 22(3):187-94. PubMed ID: 11559860
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  • 15. Mutations in the RPGR gene cause X-linked cone dystrophy.
    Yang Z, Peachey NS, Moshfeghi DM, Thirumalaichary S, Chorich L, Shugart YY, Fan K, Zhang K.
    Hum Mol Genet; 2002 Mar 01; 11(5):605-11. PubMed ID: 11875055
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  • 16. 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 01; 47(6):935-40. PubMed ID: 2239970
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  • 17. A family with RP3 type of X-linked retinitis pigmentosa: an association with ciliary abnormalities.
    van Dorp DB, Wright AF, Carothers AD, Bleeker-Wagemakers EM.
    Hum Genet; 1992 Jan 01; 88(3):331-4. PubMed ID: 1733835
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