Figure 2From: Cutis Aplasia as a clinical hallmark for the syndrome associated with 19q13.11 deletion: the possible role for UBA2 gene Schematic representation of the 13.11 deletions at the long arm of chromosome 19. Representation of eight cases with 19q13.11 deletion, evidencing the MOR region (chr19: 35,111,870-35,436,076) and the genes present. The UBA2 gene location (GRCh37:34,919,268-34,960,798) is highlighted in yellow.Back to article page