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出版商更正:使用循环游离胎儿DNA对多种孟德尔单基因疾病进行无创产前测序。

Publisher Correction: Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.

作者信息

Zhang Jinglan, Li Jianli, Saucier Jennifer B, Feng Yanming, Jiang Yanjun, Sinson Jefferson, McCombs Anne K, Schmitt Eric S, Peacock Sandra, Chen Stella, Dai Hongzheng, Ge Xiaoyan, Wang Guoli, Shaw Chad A, Mei Hui, Breman Amy, Xia Fan, Yang Yaping, Purgason Anne, Pourpak Alan, Chen Zhao, Wang Xia, Wang Yue, Kulkarni Shashikant, Choy Kwong Wai, Wapner Ronald J, Van den Veyver Ignatia B, Beaudet Arthur, Parmar Sheetal, Wong Lee-Jun, Eng Christine M

机构信息

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

Baylor Genetics, Houston, TX, USA.

出版信息

Nat Med. 2019 Apr;25(4):701-702. doi: 10.1038/s41591-019-0391-9.

DOI:10.1038/s41591-019-0391-9
PMID:30787481
Abstract

In the version of this article originally published, some cases that were presented in Fig. 3 should have been underlined but were not. The appropriate cases have now been underlined. The error has been corrected in the print, PDF and HTML versions of the article.

摘要

在本文最初发表的版本中,图3中呈现的一些病例本应加下划线,但实际未加。现在已对相应病例加上了下划线。该错误已在文章的印刷版、PDF版和HTML版中得到更正。

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引用本文的文献

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[Genetic characteristics of microtia-associated syndromes in neonates].[新生儿小耳畸形相关综合征的遗传特征]
Zhongguo Dang Dai Er Ke Za Zhi. 2022 Jun 15;24(6):614-619. doi: 10.7499/j.issn.1008-8830.2203008.