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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (5)
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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, aniridia21352 Anterior segment dysgenesis in the eyes of mice deficient for the high-mobility-group transcription factor Sox11
Wurm A; Sock E; Fuchshofer R; Wegner M; Tamm ER
Experimental Eye Research 2008; 86: 895-907
21064 Variability of clinical manifestations in the family with Axenfeld-Rieger syndrome
Kaminska A; Sokolowska-Oracz A; Pawluczyk-Dyjecinska M; Szaflik JP
Klinika Oczna 2007; 109: 321-326
20917 Aniridia with preserved visual function: A report of four cases with no mutations in PAX6
Traboulsi EI; Ellison J; Sears J; Maumenee IH; Avallone J; Mohney BG
American Journal of Ophthalmology 2008; 145: 760-764
21350 Clinical features of aniridia
Yu WH; Dong FT; Li JZ; Mao J
Zhonghua Yan Ke Za Zhi 2008; 44: 46-49
21176 Deletion of G protein-coupled receptor 48 leads to ocular anterior segment dysgenesis (ASD) through down-regulation of Pitx2
Weng J; Luo J; Cheng X; Jin C; Zhou X; Qu J; Tu L; Ai D; Li D; Wang J
Proceedings of the National Academy of Sciences of the United States of America 2008; 105: 6081-6086
