Fig. 1From: Concurrent somatic KRAS mutation and germline 10q22.3-q23.2 deletion in a patient with juvenile myelomonocytic leukemia, developmental delay, and multiple malformations: a case reportFacial feature (a) and club feet (b) of the patient. The somatic KRAS mutation on twelfth codon (arrow marked) of the patient and diseases caused by neighboring condon mutations are shown (c)Back to article page