Congenital Cataracts and Genetic Anomalies of the Lens
Author:
Publisher
Elsevier
Reference144 articles.
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3. Deletion in the Promoter Region and Altered Expression of Pitx3 Homeobox Gene in Aphakia Mice;Semina;Hum. Mol. Genet.,2000
4. Homozygous Nonsense Mutation in the FOXE3 Gene as a Cause of Congenital Primary Aphakia in Humans;Valleix;Am. J. Hum. Genet.,2006
5. Reduced TFAP2A Function Causes Variable Optic Fissure Closure and Retinal Defects and Sensitizes Eye Development to Mutations in Other Morphogenetic Regulators;Gestri;Hum. Genet.,2009
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