These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 19035245)

  • 21. Genetic linkage analyses and Cx50 mutation detection in a large multiplex Chinese family with hereditary nuclear cataract.
    He W; Li X; Chen J; Xu L; Zhang F; Dai Q; Cui H; Wang DM; Yu J; Hu S; Lu S
    Ophthalmic Genet; 2011 Mar; 32(1):48-53. PubMed ID: 21174522
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Cerulean cataract mapped to 12q13 and associated with a novel initiation codon mutation in MIP.
    Xiao X; Li W; Wang P; Li L; Li S; Jia X; Sun W; Guo X; Zhang Q
    Mol Vis; 2011; 17():2049-55. PubMed ID: 21850180
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A substitution of arginine to lysine at the COOH-terminus of MIP caused a different binocular phenotype in a congenital cataract family.
    Lin H; Hejtmancik JF; Qi Y
    Mol Vis; 2007 Sep; 13():1822-7. PubMed ID: 17960133
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family.
    Vanita V; Singh JR; Hejtmancik JF; Nuernberg P; Hennies HC; Singh D; Sperling K
    Mol Vis; 2006 May; 12():518-22. PubMed ID: 16735993
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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. PubMed ID: 9002669
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Evidence for a novel autosomal dominant retinitis pigmentosa linked to chromosome 1p22.1-q12 in a Chinese family.
    Yuan Y; Zhou X; Wang F; Yan M; Ding F
    Curr Eye Res; 2011 Feb; 36(2):154-67. PubMed ID: 21281067
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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. PubMed ID: 9199569
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel mutation in the GJA3 (connexin46) gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family.
    Yang G; Xing B; Liu G; Lu X; Jia X; Lu X; Wang X; Yu H; Fu Y; Zhao J
    Mol Vis; 2011 Apr; 17():1070-3. PubMed ID: 21552498
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A novel GJA8 mutation (p.I31T) causing autosomal dominant congenital cataract in a Chinese family.
    Wang K; Wang B; Wang J; Zhou S; Yun B; Suo P; Cheng J; Ma X; Zhu S
    Mol Vis; 2009 Dec; 15():2813-20. PubMed ID: 20019893
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Congenital anterior polar cataract associated with a missense mutation in the human alpha crystallin gene CRYAA.
    Zhang L; Zhang Y; Liu P; Cao W; Tang X; Su S
    Mol Vis; 2011; 17():2693-7. PubMed ID: 22065922
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A novel COL4A1 gene mutation results in autosomal dominant non-syndromic congenital cataract in a Chinese family.
    Xia XY; Li N; Cao X; Wu QY; Li TF; Zhang C; Li WW; Cui YX; Li XJ; Xue CY
    BMC Med Genet; 2014 Aug; 15():97. PubMed ID: 25124159
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A recurrent mutation in CRYBA1 is associated with an autosomal dominant congenital nuclear cataract disease in a Chinese family.
    Yang G; Zhai X; Zhao J
    Mol Vis; 2011; 17():1559-63. PubMed ID: 21686330
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mapping of a novel locus associated with autosomal recessive congenital cataract to chromosome 8p.
    Sabir N; Riazuddin SA; Kaul H; Iqbal F; Nasir IA; Zafar AU; Qazi ZA; Butt NH; Khan SN; Husnain T; Hejtmancik JF; Riazuddin S
    Mol Vis; 2010 Dec; 16():2911-5. PubMed ID: 21203409
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel mutation in the MIP gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family.
    Yang G; Zhang G; Wu Q; Zhao J
    Mol Vis; 2011; 17():1320-3. PubMed ID: 21647270
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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. PubMed ID: 19004499
    [TBL] [Abstract][Full Text] [Related]  

  • 36. An autosomal dominant cataract locus mapped to 19q13-qter in a Chinese family.
    Zhao R; Yang Y; He X; Liu Z; Wang P; Zhou L; Tang J; Xu W; Li L; Zhu Y
    Mol Vis; 2011 Jan; 17():265-9. PubMed ID: 21283564
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A new locus for autosomal recessive nuclear cataract mapped to chromosome 19q13 in a Pakistani family.
    Riazuddin SA; Yasmeen A; Zhang Q; Yao W; Sabar MF; Ahmed Z; Riazuddin S; Hejtmancik JF
    Invest Ophthalmol Vis Sci; 2005 Feb; 46(2):623-6. PubMed ID: 15671291
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Autosomal recessive juvenile onset cataract associated with mutation in BFSP1.
    Ramachandran RD; Perumalsamy V; Hejtmancik JF
    Hum Genet; 2007 May; 121(3-4):475-82. PubMed ID: 17225135
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Two Chinese families with pulverulent congenital cataracts and deltaG91 CRYBA1 mutations.
    Lu S; Zhao C; Jiao H; Kere J; Tang X; Zhao F; Zhang X; Zhao K; Larsson C
    Mol Vis; 2007 Jul; 13():1154-60. PubMed ID: 17653060
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A novel mutation in the connexin 50 gene (GJA8) associated with autosomal dominant congenital nuclear cataract in a Chinese family.
    Gao X; Cheng J; Lu C; Li X; Li F; Liu C; Zhang M; Zhu S; Ma X
    Curr Eye Res; 2010 Jul; 35(7):597-604. PubMed ID: 20597646
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.