Fig. 2From: Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactylyCCA phenotypes of eight affected family members. The photos of clubbed fingers from II-3, II-5, II-7, III-3; III-4, III-5, III-7 and IV-1 were taken when the samples were collectedBack to article page