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. Author manuscript; available in PMC: 2012 Jan 14.
Published in final edited form as: Clin Chim Acta. 2010 Oct 4;412(1-2):170–175. doi: 10.1016/j.cca.2010.09.035

Fig. 1.

Fig. 1

The pedigree structure of a family affected with CHD. The affected individuals are indicated by filled squares (males), and normal individuals are shown with empty squares (males) or circles (females). The deceased individual with sudden death is shown with “/”, and the proband is indicated by an arrow. +, wild type NKX2.5 allele; Ins, mutant NKX2.5 with the 2 bp insertion.