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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (2)

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11237 Axenfeld-Rieger anomaly: a novel mutation in the forkhead box C1 (FOXC1) gene in a 4-generation family
Mortemousque B; Amati-Bonneau P; Couture F; Graffan R; Dubois S; Colin J; Bonneau D; Morissette J; Lacombe D; Raymond V
Archives of Ophthalmology 2004; 122: 1527-1533

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11507 Ocular and nonocular findings in patients with aniridia
Valenzuela A; Cline RA
Canadian Journal of Ophthalmology 2004; 39: 632-638

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