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Nemer G 1

Showing records 1 to 1 | Display all abstracts from Nemer G

74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Khalil A; Al-Haddad C; Hariri H; Shibbani K; Bitar F; Kurban M; Nemer G; Arabi M
Frontiers in cardiovascular medicine 2017; 4: 58

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