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. Author manuscript; available in PMC: 2014 Jul 30.
Published in final edited form as: Annu Rev Genomics Hum Genet. 2013 Jul 15;14:355–369. doi: 10.1146/annurev-genom-091212-153523

Figure 2.

Figure 2

Clinical images of patients with RASopathies. (a) A young boy who has a clinical diagnosis of neurofibromatosis type 1. (b) A young girl with Noonan syndrome who has a PTPN11 mutation. (c) A young adult woman with Costello syndrome who has the common p.G12S HRAS mutation. (d) A school-age boy with cardio-facio-cutaneous syndrome who has a MEK2 mutation.