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Journal Abstract Search

543 related items for PubMed ID: 17197537

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  • 5. Structural assessment of PITX2, FOXC1, CYP1B1, and GJA1 genes in patients with Axenfeld-Rieger syndrome with developmental glaucoma.
    Cella W, de Vasconcellos JP, de Melo MB, Kneipp B, Costa FF, Longui CA, Costa VP.
    Invest Ophthalmol Vis Sci; 2006 May; 47(5):1803-9. PubMed ID: 16638984
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  • 6. Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions.
    Lehmann OJ, Ebenezer ND, Ekong R, Ocaka L, Mungall AJ, Fraser S, McGill JI, Hitchings RA, Khaw PT, Sowden JC, Povey S, Walter MA, Bhattacharya SS, Jordan T.
    Invest Ophthalmol Vis Sci; 2002 Jun; 43(6):1843-9. PubMed ID: 12036988
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  • 9. Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome.
    Wang X, Liu X, Huang L, Fang S, Jia X, Xiao X, Li S, Guo X.
    Curr Eye Res; 2018 Nov; 43(11):1334-1341. PubMed ID: 29939776
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  • 14. A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma.
    Micheal S, Siddiqui SN, Zafar SN, Villanueva-Mendoza C, Cortés-González V, Khan MI, den Hollander AI.
    PLoS One; 2016 Nov; 11(7):e0160016. PubMed ID: 27463523
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  • 15. A novel mutation in the FOXC1 gene in a family with Axenfeld-Rieger syndrome and Peters' anomaly.
    Weisschuh N, Wolf C, Wissinger B, Gramer E.
    Clin Genet; 2008 Nov; 74(5):476-80. PubMed ID: 18498376
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