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Journal Abstract Search

317 related items for PubMed ID: 12714612

  • 1. 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. 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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  • 5. [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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  • 6. Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.
    Ramprasad VL, Sripriya S, Ronnie G, Nancarrow D, Saxena S, Hemamalini A, Kumar D, Vijaya L, Kumaramanickavel G.
    Mol Vis; 2005 Nov 03; 11():934-40. PubMed ID: 16288197
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  • 7. 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 03; 49(9):3768-78. PubMed ID: 18421076
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  • 11. 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 03; 45(9):2879-85. PubMed ID: 15326098
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  • 13. 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 03; 14():2566-74. PubMed ID: 19122830
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  • 14. Linkage replication of the MYP12 locus in common myopia.
    Chen CY, Stankovich J, Scurrah KJ, Garoufalis P, Dirani M, Pertile KK, Richardson AJ, Baird PN.
    Invest Ophthalmol Vis Sci; 2007 Oct 03; 48(10):4433-9. PubMed ID: 17898262
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  • 16. 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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  • 17. Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.
    Nürnberg G, Jacobi FK, Broghammer M, Becker C, Blin N, Nürnberg P, Stephani U, Pusch CM.
    Int J Mol Med; 2008 Apr 29; 21(4):429-38. PubMed ID: 18360688
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  • 18. 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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  • 20. Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12.
    Stambolian D, Ibay G, Reider L, Dana D, Moy C, Schlifka M, Holmes T, Ciner E, Bailey-Wilson JE.
    Am J Hum Genet; 2004 Sep 17; 75(3):448-59. PubMed ID: 15273935
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