Fig. 2From: Intrauterine phenotype features of fetuses with 7q11.23 microduplication syndromeThe breakpoints and covered genes of each microduplication of the seven fetuses, including the well-known OMIM disease-causing gene ELN (130,160) and NCF1 (608,512). All the cases consisted of typical deletions (1.40–1.55 Mb)Back to article page