Fig. 1From: Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactylyPedigree of the family that took part in this study. The patients with congenital contractural arachnodactyly are depicted by black symbols. The arrow indicates the proband. The squares denote males and circles denote females. Crossed lines indicate deceased family membersBack to article page