Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 366


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. doi: 10.1038/eye.2011.215.


Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.

Dansault A, David G, Schwartz C, Jaliffa C, Vieira V, de la Houssaye G, Bigot K, Catin F, Tattu L, Chopin C, Halimi P, Roche O, Van Regemorter N, Munier F, Schorderet D, Dufier JL, Marsac C, Ricquier D, Menasche M, Penfornis A, Abitbol M.

Mol Vis. 2007 Apr 2;13:511-23.


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 19;17:548-57.


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 15;16:676-81.


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.


Comparison between aniridia with and without PAX6 mutations: clinical and molecular analysis in 14 Korean patients with aniridia.

Lim HT, Seo EJ, Kim GH, Ahn H, Lee HJ, Shin KH, Lee JK, Yoo HW.

Ophthalmology. 2012 Jun;119(6):1258-64. doi: 10.1016/j.ophtha.2011.12.010.


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 30;13:1555-61.


PAX6 analysis of one family and one sporadic patient from southern China with classic aniridia.

Lin Y, Liu X, Liang X, Li B, Jiang S, Ye S, Yang H, Lou B, Liu Y.

Mol Vis. 2011;17:3116-20.


A novel PAX6 mutation in a large Chinese family with aniridia and congenital cataract.

Cai F, Zhu J, Chen W, Ke T, Wang F, Tu X, Zhang Y, Jin R, Wu X.

Mol Vis. 2010 Jun 22;16:1141-5.


Mutation analysis of paired box 6 gene in inherited aniridia in northern China.

Chen P, Zang X, Sun D, Wang Y, Wang Y, Zhao X, Zhang M, Xie L.

Mol Vis. 2013;19:1169-77.


A novel PAX6 deletion in a Chinese family with congenital aniridia.

Chen JH, Lin W, Sun G, Huang C, Huang Y, Chen H, Pang CP, Zhang M.

Mol Vis. 2012;18:989-95.


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 7;12:644-8.


Mutation analysis of PAX6 in inherited and sporadic aniridia from northeastern China.

Kang Y, Lin Y, Li X, Wu Q, Huang L, Li Q, Hu Q.

Mol Vis. 2012;18:1750-4.


PAX6 analysis of two sporadic patients from southern China with classic aniridia.

Lin Y, Liu X, Yu S, Luo L, Liang X, Wang Z, Chen C, Zhu Y, Ye S, Yan H, Liu Y.

Mol Vis. 2012;18:2190-4.


Molecular genetics of familial nystagmus complicated with cataract and iris anomalies.

Yan N, Zhao Y, Wang Y, Xie A, Huang H, Yu W, Liu X, Cai SP.

Mol Vis. 2011;17:2612-7.


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 19;53(10):6338-42.


A novel PAX6 mutation in Chinese patients with severe congenital aniridia.

He Y, Pan Z, Luo F.

Curr Eye Res. 2012 Oct;37(10):879-83. doi: 10.3109/02713683.2012.688165.


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 22;15:2139-45.

Items per page

Supplemental Content

Support Center