Fig. 3From: Novel NOG (p.P42S) mutation causes proximal symphalangism in a four-generation Chinese familyIdentification of a novel NOG mutation. DNA sequencing profile around the position c.C124. The proband’s mother (III: 6) is a normal individual without SYM1. The red rectangle indicates the heterozygous mutation in the proband (IV: 6) and her affected family (II: 4, III:1, III:4, III:5)Back to article page