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Journal Abstract Search

380 related items for PubMed ID: 23954869

  • 1.
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  • 2. A family with autosomal dominant primary congenital cataract associated with a CRYGC mutation: evidence of clinical heterogeneity.
    Gonzalez-Huerta LM, Messina-Baas OM, Cuevas-Covarrubias SA.
    Mol Vis; 2007 Jul 26; 13():1333-8. PubMed ID: 17679936
    [Abstract] [Full Text] [Related]

  • 3. Mutation analysis of CRYAA, CRYGC, and CRYGD associated with autosomal dominant congenital cataract in Brazilian families.
    Santana A, Waiswol M, Arcieri ES, Cabral de Vasconcellos JP, Barbosa de Melo M.
    Mol Vis; 2009 Jul 26; 15():793-800. PubMed ID: 19390652
    [Abstract] [Full Text] [Related]

  • 4. A novel human CRYGD mutation in a juvenile autosomal dominant cataract.
    Roshan M, Vijaya PH, Lavanya GR, Shama PK, Santhiya ST, Graw J, Gopinath PM, Satyamoorthy K.
    Mol Vis; 2010 May 22; 16():887-96. PubMed ID: 20508808
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  • 6. CRYGD gene analysis in a family with autosomal dominant congenital cataract: evidence for molecular homogeneity and intrafamilial clinical heterogeneity in aculeiform cataract.
    Zenteno JC, Morales ME, Moran-Barroso V, Sanchez-Navarro A.
    Mol Vis; 2005 Jun 30; 11():438-42. PubMed ID: 16030500
    [Abstract] [Full Text] [Related]

  • 7. Novel mutation in the gamma-S crystallin gene causing autosomal dominant cataract.
    Vanita V, Singh JR, Singh D, Varon R, Sperling K.
    Mol Vis; 2009 Jun 30; 15():476-81. PubMed ID: 19262743
    [Abstract] [Full Text] [Related]

  • 8. [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 30; 48(8):713-7. PubMed ID: 23141511
    [Abstract] [Full Text] [Related]

  • 9. A missense mutation in the gammaD-crystallin gene CRYGD associated with autosomal dominant congenital cataract in a Chinese family.
    Gu F, Li R, Ma XX, Shi LS, Huang SZ, Ma X.
    Mol Vis; 2006 Jan 10; 12():26-31. PubMed ID: 16446699
    [Abstract] [Full Text] [Related]

  • 10. A mutation in GJA8 (p.P88Q) is associated with "balloon-like" cataract with Y-sutural opacities in a family of Indian origin.
    Vanita V, Singh JR, Singh D, Varon R, Sperling K.
    Mol Vis; 2008 Jun 17; 14():1171-5. PubMed ID: 18587493
    [Abstract] [Full Text] [Related]

  • 11.
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  • 12. A missense mutation in CRYGD linked with autosomal dominant congenital cataract of aculeiform type.
    Vanita V, Singh D.
    Mol Cell Biochem; 2012 Sep 17; 368(1-2):167-72. PubMed ID: 22669729
    [Abstract] [Full Text] [Related]

  • 13. A novel mutation in γD-crystallin associated with autosomal dominant congenital cataract in a Chinese family.
    Wang L, Chen X, Lu Y, Wu J, Yang B, Sun X.
    Mol Vis; 2011 Mar 26; 17():804-9. PubMed ID: 21527994
    [Abstract] [Full Text] [Related]

  • 14. Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8.
    Hansen L, Yao W, Eiberg H, Kjaer KW, Baggesen K, Hejtmancik JF, Rosenberg T.
    Invest Ophthalmol Vis Sci; 2007 Sep 26; 48(9):3937-44. PubMed ID: 17724170
    [Abstract] [Full Text] [Related]

  • 15. A novel nonsense mutation in CRYGC is associated with autosomal dominant congenital nuclear cataracts and microcornea.
    Zhang L, Fu S, Ou Y, Zhao T, Su Y, Liu P.
    Mol Vis; 2009 Sep 26; 15():276-82. PubMed ID: 19204787
    [Abstract] [Full Text] [Related]

  • 16. A novel mutation impairing the tertiary structure and stability of γC-crystallin (CRYGC) leads to cataract formation in humans and zebrafish lens.
    Li XQ, Cai HC, Zhou SY, Yang JH, Xi YB, Gao XB, Zhao WJ, Li P, Zhao GY, Tong Y, Bao FC, Ma Y, Wang S, Yan YB, Lu CL, Ma X.
    Hum Mutat; 2012 Feb 26; 33(2):391-401. PubMed ID: 22052681
    [Abstract] [Full Text] [Related]

  • 17. A nonsense mutation of CRYGC associated with autosomal dominant congenital nuclear cataracts and microcornea in a Chinese pedigree.
    Guo Y, Su D, Li Q, Yang Z, Ma Z, Ma X, Zhu S.
    Mol Vis; 2012 Feb 26; 18():1874-80. PubMed ID: 22876111
    [Abstract] [Full Text] [Related]

  • 18. Two affected siblings with nuclear cataract associated with a novel missense mutation in the CRYGD gene.
    Messina-Baas OM, Gonzalez-Huerta LM, Cuevas-Covarrubias SA.
    Mol Vis; 2006 Aug 24; 12():995-1000. PubMed ID: 16943771
    [Abstract] [Full Text] [Related]

  • 19. Novel human CRYGD rare variant in a Brazilian family with congenital cataract.
    de Figueirêdo ES, Giordano GG, Tavares A, da Silva MJ, de Vasconcellos JP, Arieta CE, de Melo MB.
    Mol Vis; 2011 Aug 24; 17():2207-11. PubMed ID: 21866214
    [Abstract] [Full Text] [Related]

  • 20. A nonsense mutation in CRYGC associated with autosomal dominant congenital nuclear cataract in a Chinese family.
    Yao K, Jin C, Zhu N, Wang W, Wu R, Jiang J, Shentu X.
    Mol Vis; 2008 Jul 09; 14():1272-6. PubMed ID: 18618005
    [Abstract] [Full Text] [Related]

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