MOESM1 of Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature

Su, Jiasun; Fu, Huayu; Xie, Bobo; Lu, Weiliang; Li, Wei; Wei, Yuan; Zhang, Qiang; Wei, Shengkai; Chen, Qiuli; Lu, Yingchi; Jiang, Tingting; Luo, Jingsi; Qin, Zailong

doi:10.6084/m9.figshare.11346074.v1

13039_2019_462_MOESM1_ESM.docx (23.56 kB)

MOESM1 of Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature

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posted on 2019-12-10, 05:09 authored 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

Additional file 1: Table S1. Thirty-six prenatal cases with pure 5p terminal deletions were reviewed from 24 published articles included our cases.

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Guangxi Zhuang Region Health Department

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Cri-du-chat syndrome Prenatal diagnosis SNP microarray Ultrasound findings

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MOESM1 of Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature

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