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The human PAX6 gene is mutated in two patients with Aniridia
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Positional cloning and characterization of a paired box- And homeobox-containing gene from the Aniridia region
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PAX6 gene dosage effects in a family with congenital cataracts, Aniridia, anophthalmia and central nervous system defects
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Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly
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Mutation of the PAX gene in patients with autosomal dominant keratitis
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