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This article [doi:10.1038/nrg1202] has been cited in the following papers, taken from those publishers and societies that are participating in CrossRef's Cited-by Linking service. The number of citations from this service is usually lower than citation numbers from databases that include more journals.

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  1. EISSN: 14602075 ISSN: 02614189

    The EMBO Journal

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    Bharesh K Chauhan et al.

    25 (10), 2006, p.2107

    doi:10.1038/sj.emboj.7601114

  2. EISSN: 15250024 ISSN: 15250016

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  3. EISSN: 1526968X ISSN: 1526954X

    genesis

    Abnormal lens morphogenesis and ectopic lens formation in the absence of β-catenin function

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    45 (4), 2007, p.157

    doi:10.1002/dvg.20277

  4. EISSN: 13616560 ISSN: 00319155

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    Dose conversion coefficients for electron exposure of the human eye lens

    R Behrens, G Dietze, M Zankl

    54 (13), 2009, p.4069

    doi:10.1088/0031-9155/54/13/008

  5. EISSN: 09697128 ISSN: 09697128

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    The developmental stage determines the distribution and duration of gene expression after early intra-amniotic gene transfer using lentiviral vectors

    M Endo et al.

    doi:10.1038/gt.2009.115

  6. EISSN: 15318249 ISSN: 03645134

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    Microphthalmia and brain atrophy: A novel neurodegenerative disease

    Øivind J. Kanavin et al.

    59 (4), 2006, p.719

    doi:10.1002/ana.20827

  7. EISSN: 1526968X ISSN: 1526954X

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    Unique contribution of heat shock transcription factor 4 in ocular lens development and fiber cell differentiation

    Jin-Na Min, Yan Zhang, Demetrius Moskophidis, Nahid F. Mivechi

    40 (4), 2004, p.205

    doi:10.1002/gene.20087

  8. EISSN: 1424859X ISSN: 14248581

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    Assignment of the PAX6 gene to bovine chromosome 15q25→q27 by fluorescence in situ hybridization and confirmation by radiation hybrid mapping

    H. Kuiper, J.L. Williams, O. Distl, C. Drögemüller

    109 (4), 2005, p.533F

    doi:10.1159/000084220

  9. EISSN: 10981004 ISSN: 10597794

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    Characterization of a familial t(16;22) balanced translocation associated with congenital cataract leads to identification of a novel gene,TMEM114, expressed in the lens and disrupted by the translocation

    Robyn V. Jamieson et al.

    28 (10), 2007, p.968

    doi:10.1002/humu.20545

  10. EISSN: 13990004 ISSN: 00099163

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    Developmental malformations of the eye: the role of PAX6, SOX2 and OTX2

    AM Hever, KA Williamson, V van Heyningen

    69 (6), 2006, p.459

    doi:10.1111/j.1399-0004.2006.00619.x

  11. EISSN: 10970223 ISSN: 01973851

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    Prenatal diagnosis of primary anophthalmia with a 3q27 interstitial deletion involving SOX2

    Agnès Guichet et al.

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    doi:10.1002/pd.997

  12. EISSN: 14382199 ISSN: 09394451

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    Eye lens proteomics

    W. Hoehenwarter, J. Klose, P. R. Jungblut

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    doi:10.1007/s00726-005-0283-9

  13. EISSN: 15376605 ISSN: 00029297

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    Heterozygous Mutations of OTX2 Cause Severe Ocular Malformations

    N RAGGE et al.

    76 (6), 2005, p.1008

    doi:10.1086/430721

  14. EISSN: 15376605 ISSN: 00029297

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    S VALLEIX et al.

    79 (2), 2006, p.358

    doi:10.1086/505654

  15. EISSN: 1435702X ISSN: 0721832X

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    244 (8), 2006, p.912

    doi:10.1007/s00417-005-0234-x

  16. EISSN: 10184813 ISSN: 10184813

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    15 (8), 2007, p.898

    doi:10.1038/sj.ejhg.5201826

  17. EISSN: 10982795 ISSN: 1040452X

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    Zebrafish mutants as models for congenital ocular disorders in humans

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  18. EISSN: 16159861 ISSN: 16159853

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    doi:10.1002/pmic.200800380

  19. EISSN: 14602083 ISSN: 09646906

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    Translational bypass of nonsense mutations in zebrafish rep1, pax2.1 and lamb1 highlights a viable therapeutic option for untreatable genetic eye disease

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    doi:10.1093/hmg/ddn302

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