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

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

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

Optic nerve dysplasia and renal insufficiency in a family with a novel PAX2 mutation, Arg115X: further ophthalmologic delineation of the renal-coloboma syndrome

By Schimmenti Lisa A.   Manligas Glenda S.   Sieving Paul A.  

Ophthalmic Genetics, Vol. 24, Iss. 4, 2003-12 ,pp. : 191-202

Informa Healthcare

Access to resources Recommend Favorite

Auditory and verbal working memory deficits in a child with congenital aniridia due to a PAX6 mutation

By Bamiou Doris-Eva   Campbell Nicole   Musiek Frank   Taylor Rachael   Chong W. K.   Moore Anthony   van Heyningen Veronica   Free Samantha   Sisodiya Sanjay   Luxon Linda  

International Journal of Audiology, Vol. 46, Iss. 4, 2007-04 ,pp. : 196-202

Informa Healthcare

Access to resources Recommend Favorite