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Strungaru MH 1
Showing records 1 to 1 | Display all abstracts from Strungaru MH17015 Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations
Strungaru MH; Dinu I; Walter MA
Investigative Ophthalmology and Visual Science 2007; 48: 228-237
