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277 related items for PubMed ID: 19204786

  • 1. Clinical and linkage study on a consanguineous Chinese family with autosomal recessive high myopia.
    Yang Z, Xiao X, Li S, Zhang Q.
    Mol Vis; 2009; 15():312-8. PubMed ID: 19204786
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  • 3. New locus for autosomal dominant high myopia maps to the long arm of chromosome 17.
    Paluru P, Ronan SM, Heon E, Devoto M, Wildenberg SC, Scavello G, Holleschau A, Mäkitie O, Cole WG, King RA, Young TL.
    Invest Ophthalmol Vis Sci; 2003 May; 44(5):1830-6. PubMed ID: 12714612
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  • 4. Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family.
    Zhang Q, Guo X, Xiao X, Yi J, Jia X, Hejtmancik JF.
    Mol Vis; 2004 Nov 17; 10():890-900. PubMed ID: 15570218
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  • 5. Genetic linkage study of high-grade myopia in a Hutterite population from South Dakota.
    Nallasamy S, Paluru PC, Devoto M, Wasserman NF, Zhou J, Young TL.
    Mol Vis; 2007 Feb 15; 13():229-36. PubMed ID: 17327828
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  • 6. [A genome-wide screening for pathological myopia suggests a novel locus on chromosome 15q12 - 13].
    Yu ZQ, Li YB, Huang CX, Chu RY, Hu DN, Shen ZH, Huang W.
    Zhonghua Yan Ke Za Zhi; 2007 Mar 15; 43(3):233-8. PubMed ID: 17605906
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  • 8. A genome-wide scan maps a novel high myopia locus to 5p15.
    Lam CY, Tam PO, Fan DS, Fan BJ, Wang DY, Lee CW, Pang CP, Lam DS.
    Invest Ophthalmol Vis Sci; 2008 Sep 15; 49(9):3768-78. PubMed ID: 18421076
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  • 12. Linkage analysis of high myopia susceptibility locus in 26 families.
    Paget S, Julia S, Vitezica ZG, Soler V, Malecaze F, Calvas P.
    Mol Vis; 2008 Sep 15; 14():2566-74. PubMed ID: 19122830
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  • 13. A new locus for autosomal recessive nuclear cataract mapped to chromosome 19q13 in a Pakistani family.
    Riazuddin SA, Yasmeen A, Zhang Q, Yao W, Sabar MF, Ahmed Z, Riazuddin S, Hejtmancik JF.
    Invest Ophthalmol Vis Sci; 2005 Feb 15; 46(2):623-6. PubMed ID: 15671291
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  • 14. 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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  • 15. Nonsyndromic high myopia in a Chinese family mapped to MYP1: linkage confirmation and phenotypic characterization.
    Guo X, Xiao X, Li S, Wang P, Jia X, Zhang Q.
    Arch Ophthalmol; 2010 Nov 15; 128(11):1473-9. PubMed ID: 21060050
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  • 16. Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1.
    Tang YG, Rabinowitz YS, Taylor KD, Li X, Hu M, Picornell Y, Yang H.
    Genet Med; 2005 Nov 15; 7(6):397-405. PubMed ID: 16024971
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  • 17. Linkage analysis of the genetic loci for high myopia on 18p, 12q, and 17q in 51 U.K. families.
    Farbrother JE, Kirov G, Owen MJ, Pong-Wong R, Haley CS, Guggenheim JA.
    Invest Ophthalmol Vis Sci; 2004 Sep 15; 45(9):2879-85. PubMed ID: 15326098
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  • 18. Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing.
    Ratnamala U, Lyle R, Rawal R, Singh R, Vishnupriya S, Himabindu P, Rao V, Aggarwal S, Paluru P, Bartoloni L, Young TL, Paoloni-Giacobino A, Morris MA, Nath SK, Antonarakis SE, Radhakrishna U.
    Invest Ophthalmol Vis Sci; 2011 Aug 29; 52(9):6814-9. PubMed ID: 21357393
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  • 19. Mapping of a novel locus associated with autosomal recessive congenital cataract to chromosome 8p.
    Sabir N, Riazuddin SA, Kaul H, Iqbal F, Nasir IA, Zafar AU, Qazi ZA, Butt NH, Khan SN, Husnain T, Hejtmancik JF, Riazuddin S.
    Mol Vis; 2010 Dec 30; 16():2911-5. PubMed ID: 21203409
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  • 20. Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1.
    Zhang Q, Guo X, Xiao X, Jia X, Li S, Hejtmancik JF.
    J Med Genet; 2006 May 30; 43(5):e20. PubMed ID: 16648373
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