Fig. 1From: MIR137 is the key gene mediator of the syndromic obesity phenotype of patients with 1p21.3 microdeletionsChromosome 1p21.3 microdeletions described to date. Minimal region of overlap highlighted by the dashed orange lines. The figure was drawn according to the UCSC Genome Browser on Human Feb. 2009 (GRCh37/hg19) assemblyBack to article page