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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (2)
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13630 PAX6 gene intragenic deletions in Mexican patients with congenital aniridiaRamirez Miranda A; Zenteno JC
Molecular Vision 2006; 12: 318-323
13743 Structural assessment of PITX2, FOXC1, CYP1B1, and GJA1 genes in patients with Axenfeld-Rieger syndrome with developmental glaucomaCella W; de Vasconcellos JP; de Melo MB; Kneipp B; Costa FF; Longui CA; Costa VP
Investigative Ophthalmology and Visual Science 2006; 47: 1803-1809
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