Figure 3From: Critical region in 2q31.2q32.3 deletion syndrome: Report of two phenotypically distinct patients, one with an additional deletion in Alagille syndrome regionPatients I and II chromosome 2 deletion compared to four previously reported patients. OMIM Morbid Map genes are in red and other genes discussed in the text are in green. The dotted black rectangle delimitates the common deleted region among the patients. Breakpoints mapped according to GRCh37, hg 19.Back to article page