Zhang, Jinglan http://orcid.org/0000-0002-4600-7123
Li, Jianli
Saucier, Jennifer B.
Feng, Yanming
Jiang, Yanjun
Sinson, Jefferson
McCombs, Anne K.
Schmitt, Eric S. http://orcid.org/0000-0002-4098-1275
Peacock, Sandra
Chen, Stella
Dai, Hongzheng
Ge, Xiaoyan
Wang, Guoli
Shaw, Chad A.
Mei, Hui
Breman, Amy http://orcid.org/0000-0003-0299-0100
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.
Article History
Received: 15 May 2018
Accepted: 17 December 2018
First Online: 28 January 2019
Change Date: 20 February 2019
Change Type: Correction
Change Details: 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.
Competing interests
: The joint venture of Department of Molecular and Human Genetics at Baylor College of Medicine (BCM) and Baylor Genetics Laboratories (BG) derives revenue from the clinical sequencing offered at BG and the authors who are BCM faculty members or BG employees are indicated in the affiliation section. J.B.S. and S.P. are employees of Natera who provided samples for validating fetal fraction calculation and contributed to the clinical data collection and analysis for the outcome study. The patent application related to this work has been filed (WO2018049049A1) by BCM and BG Laboratories, including laboratory methods of non-invasive prenatal testing to detect dominant monogenic disorders.