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bibliographicCitation Erdal E, Erdal C, Bulut G, Kunter I, Kir M, Atabey N, Açikel U. Mutation analysis of the Vangl2 coding region revealed no common cause for Tetralogy of Fallot. J Int Med Res. 2007 Nov;35(6):867–72. doi: 10.1177/147323000703500614. PMID: 18034999.
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title Mutation Analysis of the Vangl2 Coding Region Revealed No Common Cause for Tetralogy of Fallot
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