Figure 3From: Kabuki syndrome: a Chinese case series and systematic review of the spectrum of mutationsSanger sequencing of Patient 1 with two de novo mutations. (A) The missense mutation c.12199C > T in Patient 1. (B, C) Both parents had no mutations at c.12199. (D) The missense mutation c.16295G > A in Patient 1. (E, F) Both parents had no mutation at c. 16295.Back to article page