Fig. 3From: Prenatal detection and molecular cytogenetic characterization of Xp deletion and Xq duplication: a case report and literature reviewA 2.97 Mb deletion on Xp22.33p22.32 and a 16.42 Mb duplication on Xq27.1q28 were identified in the mother (A) and no significant abnormality was found on the father's X chromosome (B)Back to article page