MOESM1 of Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature
journal contributionposted on 10.12.2019 by Jiasun Su, Huayu Fu, Bobo Xie, Weiliang Lu, Wei Li, Yuan Wei, Qiang Zhang, Shengkai Wei, Qiuli Chen, Yingchi Lu, Tingting Jiang, Jingsi Luo, Zailong Qin
Any type of content formally published in an academic journal, usually following a peer-review process.
Additional file 1: Table S1. Thirty-six prenatal cases with pure 5p terminal deletions were reviewed from 24 published articles included our cases.