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Journal Abstract Search

179 related items for PubMed ID: 23141511

  • 1. [Gene mapping and analysis of candidate genes in a Chinese family with autosomal dominant congenital coralliform cataract].
    Ju H, Zhao KX, Wang LM, Wang YC, Ying M, Gao X.
    Zhonghua Yan Ke Za Zhi; 2012 Aug; 48(8):713-7. PubMed ID: 23141511
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  • 6. A missense mutation in the gammaD crystallin gene (CRYGD) associated with autosomal dominant "coral-like" cataract linked to chromosome 2q.
    Mackay DS, Andley UP, Shiels A.
    Mol Vis; 2004 Mar 17; 10():155-62. PubMed ID: 15041957
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  • 9. A recurrent mutation in CRYGD is associated with autosomal dominant congenital coralliform cataract in two unrelated Chinese families.
    Yang G, Xiong C, Li S, Wang Y, Zhao J.
    Mol Vis; 2011 Apr 28; 17():1085-9. PubMed ID: 21552497
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  • 16. 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 Apr 28; 14():1906-11. PubMed ID: 18958306
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  • 19. Crystalline cataract caused by a heterozygous missense mutation in γD-crystallin (CRYGD).
    VanderVeen DK, Andrews C, Nihalani BR, Engle EC.
    Mol Vis; 2011 Apr 28; 17():3333-8. PubMed ID: 22219628
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