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Non-Invasive Prenatal Sequencing For Multiple Mendelian Monogenic Disorders Using Circulating Cell-Free Fetal Dna (Vol 25, Pg 439, 2019)

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

NATURE MEDICINE（2019）

Cited 167|Views70
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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.
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Key words
Diagnostic markers,Genetic testing,Next-generation sequencing,Biomedicine,general,Cancer Research,Metabolic Diseases,Infectious Diseases,Molecular Medicine,Neurosciences
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