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Journal Abstract Search

236 related items for PubMed ID: 21281067

  • 1. Evidence for a novel autosomal dominant retinitis pigmentosa linked to chromosome 1p22.1-q12 in a Chinese family.
    Yuan Y, Zhou X, Wang F, Yan M, Ding F.
    Curr Eye Res; 2011 Feb; 36(2):154-67. PubMed ID: 21281067
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  • 2. Clinical and genetic identification of a large chinese family with autosomal dominant retinitis pigmentosa.
    Yang Y, Tian D, Lee J, Zeng J, Zhang H, Chen S, Guo H, Xiong Z, Xia K, Hu Z, Luo J.
    Ophthalmic Genet; 2015 Mar; 36(1):64-9. PubMed ID: 23834559
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  • 3. An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17q.
    Bardien S, Ebenezer N, Greenberg J, Inglehearn CF, Bartmann L, Goliath R, Beighton P, Ramesar R, Bhattacharya SS.
    Hum Mol Genet; 1995 Aug; 4(8):1459-62. PubMed ID: 7581389
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  • 5. A ninth locus (RP18) for autosomal dominant retinitis pigmentosa maps in the pericentromeric region of chromosome 1.
    Xu SY, Schwartz M, Rosenberg T, Gal A.
    Hum Mol Genet; 1996 Aug; 5(8):1193-7. PubMed ID: 8842740
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  • 6. Mutations in ASCC3L1 on 2q11.2 are associated with autosomal dominant retinitis pigmentosa in a Chinese family.
    Li N, Mei H, MacDonald IM, Jiao X, Hejtmancik JF.
    Invest Ophthalmol Vis Sci; 2010 Feb; 51(2):1036-43. PubMed ID: 19710410
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  • 8. Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4.
    Zhang Q, Zulfiqar F, Xiao X, Riazuddin SA, Ayyagari R, Sabar F, Caruso R, Sieving PA, Riazuddin S, Hejtmancik JF.
    Hum Genet; 2005 Dec; 118(3-4):356-65. PubMed ID: 16189710
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  • 12. Confirmation of linkage and refinement of the RP28 locus for autosomal recessive retinitis pigmentosa on chromosome 2p14-p15 in an Indian family.
    Kumar A, Shetty J, Kumar B, Blanton SH.
    Mol Vis; 2004 Jun 15; 10():399-402. PubMed ID: 15215745
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  • 13. A novel locus for autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family maps to chromosome 2p.
    Naz S, Riazuddin SA, Li L, Shahid M, Kousar S, Sieving PA, Hejtmancik JF, Riazuddin S.
    Am J Ophthalmol; 2010 May 15; 149(5):861-6. PubMed ID: 20227676
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  • 14. Gene mapping of autosomal dominant retinitis pigmentosa in a Chinese family.
    Dai LL, Sun DW, Wang Z, Fu SB, Huang SZ, Zhang ZY, Zeng G, Peng SM.
    Chin Med J (Engl); 2009 May 05; 122(9):1097-101. PubMed ID: 19493447
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  • 15. Confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3-q32.1.
    Li L, Xiao X, Yi C, Jiao X, Guo X, Hejtmancik JF, Zhang Q.
    J Hum Genet; 2012 Dec 05; 57(12):756-9. PubMed ID: 22914672
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  • 17. Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation.
    Zhang Q, Zulfiqar F, Riazuddin SA, Xiao X, Ahmad Z, Riazuddin S, Hejtmancik JF.
    Mol Vis; 2004 Nov 17; 10():884-9. PubMed ID: 15570217
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  • 19. A new locus (RP31) for autosomal dominant retinitis pigmentosa maps to chromosome 9p.
    Papaioannou M, Chakarova CF, Prescott DC, Waseem N, Theis T, Lopez I, Gill B, Koenekoop RK, Bhattacharya SS.
    Hum Genet; 2005 Dec 17; 118(3-4):501-3. PubMed ID: 16189705
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  • 20. An autosomal dominant retinitis pigmentosa family with close linkage to D7S480 on 7q.
    Millán JM, Martínez F, Vilela C, Beneyto M, Prieto F, Nájera C.
    Hum Genet; 1995 Aug 17; 96(2):216-8. PubMed ID: 7635473
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