Fig. 1From: A novel deletion mutation in KMT2A identified in a child with ID/DD and blood eosinophiliaPhotographs of the affected boy and the pedigree of his family. (a) Facial appearance of the child at 3.5 (left panel) and 5.5 (right panel) years old, respectively. (b) The filled square represents the affected proband, empty symbols represent unaffected individuals, square represents male; the circle, femaleBack to article page