Fig. 3From: Genetic heterogeneity of patients with suspected Silver-Russell syndrome: genome-wide copy number analysis in 82 patients without imprinting defectsPhotographs of patients with pathogenic copy number variations. a Patient 3 (SRS-compatible, 19q13.11 deletion syndrome). The patient had cutis aplasia over the occiput, which is characteristic of 19q13.11 deletion syndrome. b Patient 4 (SRS-like, Williams syndrome)Back to article page