Fig. 3From: Clinical and genetic findings in patients with congenital cataract and heart diseasesPathogenic genomic alterations detected in family-trios with CC and CHD. A 21q11.2-q22.3 duplication detected using aCGH in patient 1. B 22q11.21 deletion detected by WES in patient 2. C GJA8 missense mutation in patient 3Back to article page