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 *

226 related articles for article (PubMed ID: 22025896)

  • 21. PAX6 aniridia and interhemispheric brain anomalies.
    Abouzeid H; Youssef MA; ElShakankiri N; Hauser P; Munier FL; Schorderet DF
    Mol Vis; 2009 Oct; 15():2074-83. PubMed ID: 19862335
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A novel duplication in the PAX6 gene in a North Indian family with aniridia.
    Goswami S; Gupta V; Srivastava A; Sihota R; Malik MA; Kaur J
    Int Ophthalmol; 2014 Dec; 34(6):1183-8. PubMed ID: 25189681
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [A novel mutation of the PAX6 gene identified in a northeastern Chinese family with congenital aniridia].
    Kang Y; Yuan HP; Li YY
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Apr; 25(2):172-5. PubMed ID: 18393239
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Two novel mutations of the PAX6 gene causing different phenotype in a cohort of Chinese patients.
    Zhang X; Tong Y; Xu W; Dong B; Yang H; Xu L; Li Y
    Eye (Lond); 2011 Dec; 25(12):1581-9. PubMed ID: 21904390
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Identification of a novel PAX6 mutation in a family with congenital aniridia].
    Li J; Zhao L; Cai XJ; Lu L; Li G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Oct; 30(5):579-81. PubMed ID: 24078574
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mutation spectrum of PAX6 in Chinese patients with aniridia.
    Zhang X; Wang P; Li S; Xiao X; Guo X; Zhang Q
    Mol Vis; 2011; 17():2139-47. PubMed ID: 21850189
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A 556 kb deletion in the downstream region of the PAX6 gene causes familial aniridia and other eye anomalies in a Chinese family.
    Cheng F; Song W; Kang Y; Yu S; Yuan H
    Mol Vis; 2011 Feb; 17():448-55. PubMed ID: 21321669
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Two novel PAX6 mutations identified in northeastern Chinese patients with aniridia.
    Yuan H; Kang Y; Shao Z; Li Y; Yang G; Xu N
    Mol Vis; 2007 Aug; 13():1555-61. PubMed ID: 17893655
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformations.
    Hanson I; Churchill A; Love J; Axton R; Moore T; Clarke M; Meire F; van Heyningen V
    Hum Mol Genet; 1999 Feb; 8(2):165-72. PubMed ID: 9931324
    [TBL] [Abstract][Full Text] [Related]  

  • 30. PAX6 mutation in association with ptosis, cataract, iris hypoplasia, corneal opacification and diabetes: a new variant of familial aniridia?
    Peter NM; Leyland M; Mudhar HS; Lowndes J; Owen KR; Stewart H
    Clin Exp Ophthalmol; 2013 Dec; 41(9):835-41. PubMed ID: 23566044
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation.
    Syrimis A; Nicolaou N; Alexandrou A; Papaevripidou I; Nicolaou M; Loukianou E; Sismani C; Malas S; Christophidou-Anastasiadou V; Tanteles GA
    Mol Med Rep; 2018 Aug; 18(2):1623-1627. PubMed ID: 29901133
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Novel mutations of the PAX6 gene identified in Chinese patients with aniridia.
    Wang P; Guo X; Jia X; Li S; Xiao X; Zhang Q
    Mol Vis; 2006 Jun; 12():644-8. PubMed ID: 16785853
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A novel PAX6 deletion in a Chinese family with congenital aniridia.
    Liu Q; Wan W; Liu Y; Liu Y; Hu Z; Guo H; Xia K; Jin X
    Gene; 2015 May; 563(1):41-4. PubMed ID: 25746674
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [R240X mutation of the PAX6 gene in a Chinese family with congenital aniridia].
    Wang LM; Ying M; Wang X; Wang YC; Hao P; Li ND
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct; 26(5):546-9. PubMed ID: 19806579
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia.
    Chang MS; Han JC; Lee J; Kwun Y; Huh R; Ki CS; Kee C; Cho SY; Jin DK
    Ann Clin Lab Sci; 2015; 45(1):90-3. PubMed ID: 25696017
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular analysis of the PAX6 gene for congenital aniridia in the Korean population: identification of four novel mutations.
    Park SH; Kim MS; Chae H; Kim Y; Kim M
    Mol Vis; 2012; 18():488-94. PubMed ID: 22393275
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Elliptical anterior iris stromal defects associated with PAX6 gene sequence changes.
    Sharan S; Mirzayans F; Footz T; Walter M; Levin AV
    J AAPOS; 2008 Aug; 12(4):340-3. PubMed ID: 18440259
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Large novel deletions detected in Chinese families with aniridia: correlation between genotype and phenotype.
    Zhang X; Zhang Q; Tong Y; Dai H; Zhao X; Bai F; Xu L; Li Y
    Mol Vis; 2011 Feb; 17():548-57. PubMed ID: 21364908
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A novel de novo PAX6 mutation in an Ashkenazi-Jewish family with aniridia.
    Bandah D; Rosenmann A; Blumenfeld A; Averbukh E; Banin E; Sharon D
    Mol Vis; 2008 Jan; 14():142-5. PubMed ID: 18334930
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A novel mutation of PAX6 in Chinese patients with new clinical features of Peters' anomaly.
    Jia X; Guo X; Jia X; Xiao X; Li S; Zhang Q
    Mol Vis; 2010 Apr; 16():676-81. PubMed ID: 20405024
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.