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Journal Abstract Search

342 related items for PubMed ID: 10909854

  • 1. An autosomal dominant posterior polar cataract locus maps to human chromosome 20p12-q12.
    Yamada K, Tomita H, Yoshiura K, Kondo S, Wakui K, Fukushima Y, Ikegawa S, Nakamura Y, Amemiya T, Niikawa N.
    Eur J Hum Genet; 2000 Jul; 8(7):535-9. PubMed ID: 10909854
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  • 2. A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.
    Bateman JB, Geyer DD, Flodman P, Johannes M, Sikela J, Walter N, Moreira AT, Clancy K, Spence MA.
    Invest Ophthalmol Vis Sci; 2000 Oct; 41(11):3278-85. PubMed ID: 11006214
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  • 3. Posterior polar cataract: genetic analysis of a large family.
    Finzi S, Li Y, Mitchell TN, Farr A, Maumenee IH, Sallum JM, Sundin O.
    Ophthalmic Genet; 2005 Sep; 26(3):125-30. PubMed ID: 16272057
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  • 4. A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts.
    Ma X, Li FF, Wang SZ, Gao C, Zhang M, Zhu SQ.
    Mol Vis; 2008 Sep; 14():1906-11. PubMed ID: 18958306
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  • 5. 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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  • 8. A novel locus for autosomal dominant nuclear cataract mapped to chromosome 2p12 in a Pakistani family.
    Khaliq S, Hameed A, Ismail M, Anwar K, Mehdi SQ.
    Invest Ophthalmol Vis Sci; 2002 Jul 17; 43(7):2083-7. PubMed ID: 12091400
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  • 10. Genetic linkage of snowflake vitreoretinal degeneration to chromosome 2q36.
    Jiao X, Ritter R, Hejtmancik JF, Edwards AO.
    Invest Ophthalmol Vis Sci; 2004 Dec 17; 45(12):4498-503. PubMed ID: 15557460
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  • 11. A novel missense mutation in the gene for gap-junction protein alpha3 (GJA3) associated with autosomal dominant "nuclear punctate" cataracts linked to chromosome 13q.
    Bennett TM, Mackay DS, Knopf HL, Shiels A.
    Mol Vis; 2004 Jun 11; 10():376-82. PubMed ID: 15208569
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  • 12. First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1.
    Vieira H, Gregory-Evans K, Lim N, Brookes JL, Brueton LA, Gregory-Evans CY.
    Invest Ophthalmol Vis Sci; 2002 Aug 11; 43(8):2540-5. PubMed ID: 12147582
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  • 14. A homozygous splice mutation in the HSF4 gene is associated with an autosomal recessive congenital cataract.
    Smaoui N, Beltaief O, BenHamed S, M'Rad R, Maazoul F, Ouertani A, Chaabouni H, Hejtmancik JF.
    Invest Ophthalmol Vis Sci; 2004 Aug 11; 45(8):2716-21. PubMed ID: 15277496
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  • 17. Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataract.
    Cohen D, Bar-Yosef U, Levy J, Gradstein L, Belfair N, Ofir R, Joshua S, Lifshitz T, Carmi R, Birk OS.
    Invest Ophthalmol Vis Sci; 2007 May 11; 48(5):2208-13. PubMed ID: 17460281
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  • 18. CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate gene.
    Danciger M, Hendrickson J, Lyon J, Toomes C, McHale JC, Fishman GA, Inglehearn CF, Jacobson SG, Farber DB.
    Invest Ophthalmol Vis Sci; 2001 Oct 11; 42(11):2458-65. PubMed ID: 11581183
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