Prospective prenatal cell-free DNA screening for genetic conditions of heterogenous etiologies
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Published:2024-01-22
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ISSN:1078-8956
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Container-title:Nature Medicine
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language:en
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Short-container-title:Nat Med
Author:
Zhang JinglanORCID, Wu YantingORCID, Chen Songchang, Luo Qiong, Xi Hui, Li Jianli, Qin Xiaomei, Peng Ying, Ma Na, Yang Bingxin, Qiu Xiang, Lu Weiliang, Chen Yuan, Jiang Ying, Chen Panpan, Liu YifengORCID, Zhang Chen, Zhang Zhiwei, Xiong Yu, Shen Jie, Liang Huan, Ren Yunyun, Ying Chunmei, Dong Minyue, Li Xiaotian, Xu Congjian, Wang Hua, Zhang DanORCID, Xu ChenmingORCID, Huang HefengORCID
Publisher
Springer Science and Business Media LLC
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Reference61 articles.
1. Congenital disorders. WHO https://www.who.int/news-room/fact-sheets/detail/birth-defects (2023). 2. Mai, C. T. et al. National population-based estimates for major birth defects, 2010–2014. Birth Defects Res. 111, 1420–1435 (2019). 3. Bacino, C. A. Congenital anomalies: epidemiology, types, and patterns. UpToDate https://www.uptodate.com/contents/birth-defects-epidemiology-types-and-patterns (2023). 4. Moore, K. L., Persaud, T. V. N. & Torchia, M. G. The Developing Human: Clinically Oriented Embryology (Elsevier Health Sciences, 2018). 5. Antonarakis, S. E. Carrier screening for recessive disorders. Nat. Rev. Genet. 20, 549–561 (2019).
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