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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (6)
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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, aniridia49319 Localization of SH3PXD2B in human eyes and detection of rare variants in patients with anterior segment diseases and glaucoma
Mao M; Solivan-Timpe F; Roos BR; Mullins RF; Oetting TA; Kwon YH; Brzeskiewicz PM; Stone EM; Alward WL; Anderson MG; Fingert JH
Molecular Vision 2012; 18: 705-713
48749 Ocular and systemic findings in a survey of aniridia subjects
Netland PA; Scott ML; Boyle JW; Lauderdale JD
Journal of AAPOS 2011; 15: 562-566
48615 PAX6 3' deletion in a family with aniridia
Wawrocka A; Budny B; Debicki S; Jamsheer A; Sowinska A; Krawczynski MR
Ophthalmic Genetics 2012; 33: 44-48
49149 A recurrent PAX6 mutation is associated with aniridia and congenital progressive cataract in a Chinese family
Jin C; Wang Q; Li J; Zhu Y; Shentu X; Yao K
Molecular Vision 2012; 18: 465-470
48842 Axenfeld-Rieger syndrome: new perspectives
Chang TC; Summers CG; Schimmenti LA; Grajewski AL
British Journal of Ophthalmology 2012; 96: 318-322
48951 Klinefelter Syndrome Associated With Goniodysgenesis
Matlach J; Grehn F; Klink T
Journal of Glaucoma 2013; 22: e7-e8
