Fig. 3From: Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutationsFacial features observed in two NS families. Family 1-Mother and daughter with the pathogenic variant c.923A > G in exon 8 of the PTPN11 gene. Family 2- Father and son with the c.922A > G pathogenic variant in exon 8 of the PTPN11 geneBack to article page