Fig. 3From: Association of GNAS imprinting defects and deletions of chromosome 2 in two patients: clues explaining phenotypic heterogeneity in pseudohypoparathyroidism type 1B/iPPSD3Representative figure from the UCSC Genome Browser resuming the extension range of previously reported BDMR-associated deletions and genes included. The smallest region of overlap (SRO) between known and our deletions is highlighted in redBack to article page