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Ophthalmic Genetics 1
Showing records 1 to 1 | Display all abstracts in Ophthalmic Genetics21575 Heterozygous FOXC1 mutation (M161K) associated with congenital glaucoma and aniridia in an infant and a milder phenotype in her mother
Khan AO; Aldahmesh MA; Al-Amri A
Ophthalmic Genetics 2008; 29: 67-71