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Journal Abstract Search

106 related items for PubMed ID: 2288459

  • 1. Exclusion of linkage between D3S47 (C17) and ADRPII gene in two large families of moderate autosomal dominant retinitis pigmentosa: evidence for genetic heterogeneity.
    Kaplan J, Guasconi G, Dufier JL, Michel-Awad A, David A, Munnich A, Frezal J.
    Ann Genet; 1990; 33(3):152-4. PubMed ID: 2288459
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  • 2. Usher syndrome type I is not linked to D1S81 (pTHH 33): evidence for genetic heterogeneity.
    Kaplan J, Guasconi G, Bonneau D, Melki J, Briard ML, Munnich A, Dufier JL, Frézal J.
    Ann Genet; 1990; 33(2):105-8. PubMed ID: 1978628
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  • 5. No evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): evidence for genetic heterogeneity.
    Inglehearn CF, Jay M, Lester DH, Bashir R, Jay B, Bird AC, Wright AF, Evans HJ, Papiha SS, Bhattacharya SS.
    Genomics; 1990 Jan; 6(1):168-73. PubMed ID: 2303257
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  • 9. Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q.
    Jordan SA, Farrar GJ, Kenna P, Humphries MM, Sheils DM, Kumar-Singh R, Sharp EM, Soriano N, Ayuso C, Benitez J.
    Nat Genet; 1993 May; 4(1):54-8. PubMed ID: 8513324
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  • 11. Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity.
    Lester DH, Inglehearn CF, Bashir R, Ackford H, Esakowitz L, Jay M, Bird AC, Wright AF, Papiha SS, Bhattacharya SS.
    Am J Hum Genet; 1990 Sep; 47(3):536-41. PubMed ID: 2393026
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  • 13. Evidence for further genetic heterogeneity in autosomal dominant retinitis pigmentosa.
    Kumar-Singh R, Kenna PF, Farrar GJ, Humphries P.
    Genomics; 1993 Jan; 15(1):212-5. PubMed ID: 8432539
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  • 16. Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3.
    McWilliam P, Farrar GJ, Kenna P, Bradley DG, Humphries MM, Sharp EM, McConnell DJ, Lawler M, Sheils D, Ryan C.
    Genomics; 1989 Oct; 5(3):619-22. PubMed ID: 2613244
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  • 17. Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.
    Riazuddin SA, Zulfiqar F, Zhang Q, Sergeev YV, Qazi ZA, Husnain T, Caruso R, Riazuddin S, Sieving PA, Hejtmancik JF.
    Invest Ophthalmol Vis Sci; 2005 Jul; 46(7):2264-70. PubMed ID: 15980210
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  • 19. Retinitis pigmentosa in Spain. The Spanish Multicentric and Multidisciplinary Group for Research into Retinitis Pigmentosa.
    Ayuso C, Garcia-Sandoval B, Najera C, Valverde D, Carballo M, Antiñolo G.
    Clin Genet; 1995 Sep; 48(3):120-2. PubMed ID: 8556816
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