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    Results: 1 to 20 of 990

    1.

    The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes.

    McKay JD, Patterson B, Craig JE, Russell-Eggitt IM, Wirth MG, Burdon KP, Hewitt AW, Cohn AC, Kerdraon Y, Mackey DA.

    Br J Ophthalmol. 2005 Jul;89(7):831-4.PMID: 15965161 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    A novel mutation in the DNA-binding domain of MAF at 16q23.1 associated with autosomal dominant "cerulean cataract" in an Indian family.

    Vanita V, Singh D, Robinson PN, Sperling K, Singh JR.

    Am J Med Genet A. 2006 Mar 15;140(6):558-66.PMID: 16470690 [PubMed - indexed for MEDLINE]Related articles

    3.

    A novel form of "central pouchlike" cataract, with sutural opacities, maps to chromosome 15q21-22.

    Vanita, Singh JR, Sarhadi VK, Singh D, Reis A, Rueschendorf F, Becker-Follmann J, Jung M, Sperling K.

    Am J Hum Genet. 2001 Feb;68(2):509-14. Epub 2000 Dec 21.PMID: 11133359 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    A new locus for congenital cataract, microcornea, microphthalmia, and atypical iris coloboma maps to chromosome 2.

    Abouzeid H, Meire FM, Osman I, ElShakankiri N, Bolay S, Munier FL, Schorderet DF.

    Ophthalmology. 2009 Jan;116(1):154-162.e1. Epub 2008 Nov 12.PMID: 19004499 [PubMed - indexed for MEDLINE]Related articles

    5.

    A locus for autosomal dominant posterior polar cataract on chromosome 1p.

    Ionides AC, Berry V, Mackay DS, Moore AT, Bhattacharya SS, Shiels A.

    Hum Mol Genet. 1997 Jan;6(1):47-51.PMID: 9002669 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    An autosomal dominant progressive congenital zonular nuclear cataract linked to chromosome 20p12.2-p11.23.

    Li N, Yang Y, Bu J, Zhao C, Lu S, Zhao J, Yan L, Cui L, Zheng R, Li J, Tang J, Zhao K.

    Mol Vis. 2006 Dec 5;12:1506-10.PMID: 17167408 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    A new locus for inherited nuclear cataract mapped to the long arm of chromosome 1.

    Wang L, Lin H, Shen Y, Huang S, Gu J, Su H, Qi Y.

    Mol Vis. 2007 Aug 1;13:1357-62.PMID: 17768382 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    A new locus for autosomal dominant posterior polar cataract in Moroccan Jews maps to chromosome 14q22-23.

    Pras E, Mahler O, Kumar V, Frydman M, Gefen N, Pras E, Hejtmancik JF.

    J Med Genet. 2006 Oct;43(10):e50.PMID: 17047090 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    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;14:1906-11. Epub 2008 Oct 24.PMID: 18958306 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Identification of a CRYAB mutation associated with autosomal dominant posterior polar cataract in a Chinese family.

    Liu M, Ke T, Wang Z, Yang Q, Chang W, Jiang F, Tang Z, Li H, Ren X, Wang X, Wang T, Li Q, Yang J, Liu J, Wang QK.

    Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3461-6.PMID: 16877416 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    A new locus for dominant "zonular pulverulent" cataract, on chromosome 13.

    Mackay D, Ionides A, Berry V, Moore A, Bhattacharya S, Shiels A.

    Am J Hum Genet. 1997 Jun;60(6):1474-8.PMID: 9199569 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    The E233del mutation in BFSP2 causes a progressive autosomal dominant congenital cataract in a Chinese family.

    Cui X, Gao L, Jin Y, Zhang Y, Bai J, Feng G, Gao W, Liu P, He L, Fu S.

    Mol Vis. 2007 Oct 24;13:2023-9.PMID: 17982427 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    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;45(8):2716-21.PMID: 15277496 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    A locus for autosomal dominant anterior polar cataract on chromosome 17p.

    Berry V, Ionides AC, Moore AT, Plant C, Bhattacharya SS, Shiels A.

    Hum Mol Genet. 1996 Mar;5(3):415-9.PMID: 8852669 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataracts.

    Li F, Wang S, Gao C, Liu S, Zhao B, Zhang M, Huang S, Zhu S, Ma X.

    Mol Vis. 2008 Mar 4;14:378-86.PMID: 18334953 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Identification of a genetic locus for autosomal dominant infantile cataract on chromosome 20p12.1-p11.23 in a Chinese family.

    Zhang S, Liu M, Dong JM, Yin K, Wang P, Bu J, Li J, Hao YS, Hao P, Wang QK, Wang L.

    Mol Vis. 2008;14:1893-7. Epub 2008 Oct 22.PMID: 18958302 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    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 3;11:934-40.PMID: 16288197 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    A novel locus of coralliform cataract mapped to chromosome 2p24-pter.

    Gao L, Qin W, Cui H, Feng G, Liu P, Gao W, Ma L, Li P, He L, Fu S.

    J Hum Genet. 2005;50(6):305-10. Epub 2005 Jun 3.PMID: 15933805 [PubMed - indexed for MEDLINE]Related articles

    19.

    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;43(7):2083-7.PMID: 12091400 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    A novel nonsense mutation in CRYBB1 associated with autosomal dominant congenital cataract.

    Yang J, Zhu Y, Gu F, He X, Cao Z, Li X, Tong Y, Ma X.

    Mol Vis. 2008 Apr 18;14:727-31.PMID: 18432316 [PubMed - indexed for MEDLINE]Related articlesFree article

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