Fig. 3From: Congenital nephrotic syndrome associated with 22q11.2 duplication syndrome in a Chinese family and functional analysis of the intronic NPHS1 c. 3286 + 5G > A mutationCMA results of the proband with CytoScan 750 K array (Affymetrix, USA), showing a 3.2 duplication on chromosome 22q11.21Back to article page