Delineation of 2q32q35 Deletion Phenotypes: Two Apparent “Proximal” and “Distal” Syndromes
Figure 2
Schematic of the chromosome 2 region encompassing the deletions detected in the patients reported here. Panel (a) shows an ideogram of chromosome 2. Panel (b) shows the OMIM genes and RefSeq genes that lie in the region of the deletions reported here. Panel (c) shows the location and extent of the deletions for patients 1, 2, and 3. The images in panels (a) and (b) are taken from the UCSC genome browser (http://genome.ucsc.edu/).
