A Novel PAX6 Mutation in Chinese Patients with Severe Congenital Aniridia

By He Yan   Pan Zhiqiang   Luo Fei  

Current Eye Research, Vol. 37, Iss. 10, 2012-10 ,pp. : 879-883

Informa Healthcare

Access to resources Recommend Favorite

Mutation Analysis of PAX6 in a Chinese Family and a Patient with a Presumed Sporadic Case of Congenital Aniridia

By  

Ophthalmic Research, Vol. 47, Iss. 1, 2011-06 ,pp. : 27-31

Karger

Access to resources Recommend Favorite

Microphthalmia, late onset keratitis, and iris coloboma/aniridia in a family with a novel PAX6 mutation

By Xiao Xueshan   Li Shiqiang   Zhang Qingjiong  

Ophthalmic Genetics, Vol. 33, Iss. 2, 2012-06 ,pp. : 119-121

Informa Healthcare

Access to resources Recommend Favorite

PAX6 3′ deletion in a family with aniridia

By Wawrocka Anna   Budny Bartlomiej   Debicki Szymon   Jamsheer Aleksander   Sowinska Anna   Krawczynski Maciej Robert  

Ophthalmic Genetics, Vol. 33, Iss. 1, 2012-03 ,pp. : 44-48

Informa Healthcare

Access to resources Recommend Favorite

Novel and De-novo Truncating PAX6 Mutations and Ocular Phenotypes in Thai Aniridia Patients

By Atchaneeyasakul La-ongsri   Trinavarat Adisak   Dulayajinda Dhaivadee   Kumpornsin Kornphet   Thongnoppakhun Wanna   Yenchitsomanus Pa-thai   Limwongse Chanin  

Ophthalmic Genetics, Vol. 27, Iss. 1, 2006-03 ,pp. : 21-27

Informa Healthcare

Access to resources Recommend Favorite