Figure 2From: Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences SPD1 phenotype in the Asian families. Radiographs and photographs showing the SPD1 phenotype in the Pakistani (A – F), and Indian (G – K) families. A-B, (subject IX-23); C-D, (IX-20); E-F, (VIII-24); G-H, (IV-7); I, (III-3); J, (V-6); K-L, (V-3). Phenotypic categories are given in Figure 3.Back to article page