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Journal Abstract Search

145 related items for PubMed ID: 7977377

  • 1. Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).
    Hong HK, Ferrell RE, Gorin MB.
    Am J Hum Genet; 1994 Dec; 55(6):1173-81. PubMed ID: 7977377
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  • 2. Linkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3.
    Seymour AB, Dash-Modi A, O'Connell JR, Shaffer-Gordon M, Mah TS, Stefko ST, Nagaraja R, Brown J, Kimura AE, Ferrell RE, Gorin MB.
    Am J Hum Genet; 1998 Jan; 62(1):122-9. PubMed ID: 9443860
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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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  • 8. Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.
    Lines MA, Hébert M, McTaggart KE, Flynn SJ, Tennant MT, MacDonald IM.
    Ophthalmology; 2002 Oct; 109(10):1862-70. PubMed ID: 12359607
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  • 9. Clinical variability in a family with X-linked retinal dystrophy and the locus at the RP3 site.
    Keith CG, Denton MJ, Chen JD.
    Ophthalmic Paediatr Genet; 1991 Jun; 12(2):91-8. PubMed ID: 1923319
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  • 10. Clinical features and a follow-up study in a family with X-linked progressive cone-rod dystrophy.
    Mäntyjärvi M, Nurmenniemi P, Partanen J, Myöhänen T, Peippo M, Alitalo T.
    Acta Ophthalmol Scand; 2001 Aug; 79(4):359-65. PubMed ID: 11453854
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  • 11. 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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  • 12. A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27.
    Gieser L, Fujita R, Göring HH, Ott J, Hoffman DR, Cideciyan AV, Birch DG, Jacobson SG, Swaroop A.
    Am J Hum Genet; 1998 Nov; 63(5):1439-47. PubMed ID: 9792872
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  • 13. Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.
    Jacobson SG, Buraczynska M, Milam AH, Chen C, Järvaläinen M, Fujita R, Wu W, Huang Y, Cideciyan AV, Swaroop A.
    Invest Ophthalmol Vis Sci; 1997 Sep; 38(10):1983-97. PubMed ID: 9331262
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  • 14. Genetic mapping of loci for X-linked retinitis pigmentosa.
    Dahl N, Sundvall M, Pettersson U, Andréasson S, Anvret M, Kugelberg U, Hagbyhn-Gericke A, Goonewardena P.
    Clin Genet; 1991 Dec; 40(6):435-40. PubMed ID: 1685699
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  • 16. Linkage heterogeneity between X-linked retinitis pigmentosa and a map of 10 RFLP loci.
    Chen JD, Halliday F, Keith G, Sheffield L, Dickinson P, Gray R, Constable I, Denton M.
    Am J Hum Genet; 1989 Sep; 45(3):401-11. PubMed ID: 2570529
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  • 17. 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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  • 18. An autosomal dominant bull's-eye macular dystrophy (MCDR2) that maps to the short arm of chromosome 4.
    Michaelides M, Johnson S, Poulson A, Bradshaw K, Bellmann C, Hunt DM, Moore AT.
    Invest Ophthalmol Vis Sci; 2003 Apr; 44(4):1657-62. PubMed ID: 12657606
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  • 19. 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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  • 20. Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt disease.
    Kniazeva MF, Chiang MF, Cutting GR, Zack DJ, Han M, Zhang K.
    Ophthalmic Genet; 1999 Jun; 20(2):71-81. PubMed ID: 10420191
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