Fig. 4From: A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphismsA schematic comparison of the chromosome 2q13 deletions identified in patient 1 and patient 2 reported in the present study and in the 27 previously published patients. The telomeric border of the deletion in patient 2 was refined by qPCR (Additional file 3: Figure S2)Back to article page