Fig. 1From: A Chinese family with Noonan syndrome caused by a heterozygous variant in LZTR1: a case report and literature reviewPedigrees of the Noonan syndrome families with variant c.1149 + 1G > T of the LZTR1 gene. The arrow indicates the proband. Black indicates that the patient exhibited variant c.1149 + 1G > T of LZTR1. Stripes indicate that the patient had a NS-like appearance to varying degrees. The numbers above the patients indicates their height.Back to article page