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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (3)
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Display all abstracts in classification 9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia
Search within classification 9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia53899 11p13 deletions can be more frequent than the PAX6 gene point mutations in Polish patients with aniridia
Wawrocka A; Sikora A; Kuszel L; Krawczynski MR
Journal of Applied Genetics 2013; 54: 345-351
53528 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
Clinical and Experimental Ophthalmology 2013; 41: 835-841
54056 Aniridia associated with lens coloboma and secondary glaucoma treated with transcorneal argon laser ciliary body photocoagulation: a case report
Sbordone S; Romano V; Savastano A; Piccirillo V; Savastano MC; Bifani M
Case Reports in Ophthalmology 2013; 4: 44-47
