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.
226 related articles for article (PubMed ID: 22025896)
41. [A novel mutation of the PAX6 gene in a Chinese family with aniridia]. Kang Y; Yuan HP; Li X; Li QJ; Wu Q; Hu Q Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug; 27(4):376-80. PubMed ID: 20677140 [TBL] [Abstract][Full Text] [Related]
42. PAX6 mutation as a genetic factor common to aniridia and glucose intolerance. Yasuda T; Kajimoto Y; Fujitani Y; Watada H; Yamamoto S; Watarai T; Umayahara Y; Matsuhisa M; Gorogawa S; Kuwayama Y; Tano Y; Yamasaki Y; Hori M Diabetes; 2002 Jan; 51(1):224-30. PubMed ID: 11756345 [TBL] [Abstract][Full Text] [Related]
43. Molecular analysis of the PAX6 gene in Mexican patients with congenital aniridia: report of four novel mutations. Villarroel CE; Villanueva-Mendoza C; Orozco L; Alcántara-Ortigoza MA; Jiménez DF; Ordaz JC; González-del Angel A Mol Vis; 2008 Sep; 14():1650-8. PubMed ID: 18776953 [TBL] [Abstract][Full Text] [Related]
44. [Analysis of PAX6 gene in a Chinese family with congenital aniridia]. Li PC; Yao Q; Ren X; Zhang MC; Li H; Liu JY; Sheng SY; Wang Q; Liu MG Zhonghua Yan Ke Za Zhi; 2009 Oct; 45(10):931-4. PubMed ID: 20137456 [TBL] [Abstract][Full Text] [Related]
45. Investigation of a PAX6 gene mutation in a Malaysian family with congenital aniridia. Lee PC; Lam HH; Ghani SA; Subrayan V; Chua KH Genet Mol Res; 2014 Mar; 13(2):3553-9. PubMed ID: 24737507 [TBL] [Abstract][Full Text] [Related]
46. Familial peripheral keratopathy without PAX6 mutation. Smith WM; Lange JM; Sturm AC; Tanner SM; Mauger TF Cornea; 2012 Feb; 31(2):130-3. PubMed ID: 22146551 [TBL] [Abstract][Full Text] [Related]
47. Microphthalmia, late onset keratitis, and iris coloboma/aniridia in a family with a novel PAX6 mutation. Xiao X; Li S; Zhang Q Ophthalmic Genet; 2012 Jun; 33(2):119-21. PubMed ID: 22171686 [TBL] [Abstract][Full Text] [Related]
48. Non-invasive anterior segment and posterior segment optical coherence tomography and phenotypic characterization of aniridia. Gregory-Evans K; Cheong-Leen R; George SM; Xie J; Moosajee M; Colapinto P; Gregory-Evans CY Can J Ophthalmol; 2011 Aug; 46(4):337-44. PubMed ID: 21816254 [TBL] [Abstract][Full Text] [Related]
49. PAX6 mutations identified in 4 of 35 families with microcornea. Wang P; Sun W; Li S; Xiao X; Guo X; Zhang Q Invest Ophthalmol Vis Sci; 2012 Sep; 53(10):6338-42. PubMed ID: 22893676 [TBL] [Abstract][Full Text] [Related]
50. A novel PAX6 gene mutation in an Indian aniridia patient. Neethirajan G; Hanson IM; Krishnadas SR; Vijayalakshmi P; Anupkumar K; Sundaresan P Mol Vis; 2003 May; 9():205-9. PubMed ID: 12789139 [TBL] [Abstract][Full Text] [Related]
51. A novel de novo duplication mutation of PAX6 in a Chinese family with aniridia and other ocular abnormalities. Zhuang J; Chen X; Tan Z; Zhu Y; Zhao K; Yang J Sci Rep; 2014 May; 4():4836. PubMed ID: 24787241 [TBL] [Abstract][Full Text] [Related]
52. Variable phenotype related to a novel PAX 6 mutation (IVS4+5G>C) in a family presenting congenital nystagmus and foveal hypoplasia. Vincent MC; Gallai R; Olivier D; Speeg-Schatz C; Flament J; Calvas P; Dollfus H Am J Ophthalmol; 2004 Dec; 138(6):1016-21. PubMed ID: 15629294 [TBL] [Abstract][Full Text] [Related]
53. Detailed ophthalmologic evaluation of 43 individuals with PAX6 mutations. Hingorani M; Williamson KA; Moore AT; van Heyningen V Invest Ophthalmol Vis Sci; 2009 Jun; 50(6):2581-90. PubMed ID: 19218613 [TBL] [Abstract][Full Text] [Related]
54. [Study of genetic mutation locus in a family with congenital aniridia]. Cong RC; Song SJ; Liu YZ Zhonghua Yan Ke Za Zhi; 2006 Dec; 42(12):1113-7. PubMed ID: 17415970 [TBL] [Abstract][Full Text] [Related]
55. Eye anomalies and neurological manifestations in patients with PAX6 mutations. Chien YH; Huang HP; Hwu WL; Chien YH; Chang TC; Lee NC Mol Vis; 2009 Oct; 15():2139-45. PubMed ID: 19898691 [TBL] [Abstract][Full Text] [Related]
57. Isolated aniridia caused by a novel Torrefranca AB; Carmona SM; Santiago APD; Cutiongco-Dela Paz E; Lingao MD Ophthalmic Genet; 2023 Oct; 44(5):501-504. PubMed ID: 36440799 [TBL] [Abstract][Full Text] [Related]
58. 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]
59. Mutation analysis of PAX6 gene in a large Chinese family with aniridia. Song SJ; Liu YZ; Cong RC; Jin Y; Hou ZQ; Ma ZZ; Ren GC; Li LS Chin Med J (Engl); 2005 Feb; 118(4):302-6. PubMed ID: 15740668 [TBL] [Abstract][Full Text] [Related]
60. A [c.566-2A>G] heterozygous mutation in the PAX6 gene causes aniridia with mild visual impairment. Beby F; Dieterich K; Calvas P Eye (Lond); 2011 May; 25(5):657-8. PubMed ID: 21274015 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]