Fig. 1From: Cardio-facio-cutaneous syndrome and gastrointestinal defects: report on a newborn with 19p13.3 deletion including the MAP 2 K2 geneOverview of the 19p13.3 region and its gene content, showing present patient’s microdeletion spanning about 1.27 Mb of genomic DNA, from position 2,980,128 to 4,251,077, according to DECIPHER Genome Browser (GRCh37/hg19 assembly) [3]Back to article page