Fig.Ā 1From: Mutations in fibroblast growth factor (FGF8) and FGF10 identified in patients with conotruncal defectsSequences of FGF8 and FGF10 mutants identified in patients with CTD and controls. a, c, e Chromatograms of normal controls. b, d Chromatograms of the two heterozygous variants. f Deletion mutation in FGF10. Arrows indicate the nucleotide changes and the deletionBack to article page