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The Journal of Maternal-Fetal & Neonatal Medicine Volume 34, 2021 - Issue 16
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Original Articles

The application of expanded noninvasive prenatal screening for genome-wide chromosomal abnormalities and genetic counseling

Yun Chena Genetic and Metabolic Central Laboratory, The Maternal and Child Health Care Hospital of Guangxi Zhuang Autonomous Region, Guangxi Birth Defects Prevention and Control Institute, Nanning, PR ChinaORCID Iconhttps://orcid.org/0000-0002-8337-9874View further author information
ORCID Icon,
Yunli Laia Genetic and Metabolic Central Laboratory, The Maternal and Child Health Care Hospital of Guangxi Zhuang Autonomous Region, Guangxi Birth Defects Prevention and Control Institute, Nanning, PR ChinaView further author information
,
Fuben Xua Genetic and Metabolic Central Laboratory, The Maternal and Child Health Care Hospital of Guangxi Zhuang Autonomous Region, Guangxi Birth Defects Prevention and Control Institute, Nanning, PR ChinaView further author information
,
Haisong Qina Genetic and Metabolic Central Laboratory, The Maternal and Child Health Care Hospital of Guangxi Zhuang Autonomous Region, Guangxi Birth Defects Prevention and Control Institute, Nanning, PR ChinaView further author information
,
Yanqing Tanga Genetic and Metabolic Central Laboratory, The Maternal and Child Health Care Hospital of Guangxi Zhuang Autonomous Region, Guangxi Birth Defects Prevention and Control Institute, Nanning, PR ChinaView further author information
,
Xiaoshan Huanga Genetic and Metabolic Central Laboratory, The Maternal and Child Health Care Hospital of Guangxi Zhuang Autonomous Region, Guangxi Birth Defects Prevention and Control Institute, Nanning, PR ChinaView further author information
,
Lintao Menga Genetic and Metabolic Central Laboratory, The Maternal and Child Health Care Hospital of Guangxi Zhuang Autonomous Region, Guangxi Birth Defects Prevention and Control Institute, Nanning, PR ChinaView further author information
,
Jiasun Sua Genetic and Metabolic Central Laboratory, The Maternal and Child Health Care Hospital of Guangxi Zhuang Autonomous Region, Guangxi Birth Defects Prevention and Control Institute, Nanning, PR ChinaView further author information
,
Weijia Suna Genetic and Metabolic Central Laboratory, The Maternal and Child Health Care Hospital of Guangxi Zhuang Autonomous Region, Guangxi Birth Defects Prevention and Control Institute, Nanning, PR ChinaView further author information
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Yiping Shena Genetic and Metabolic Central Laboratory, The Maternal and Child Health Care Hospital of Guangxi Zhuang Autonomous Region, Guangxi Birth Defects Prevention and Control Institute, Nanning, PR China;b Division of Genetics and Genomics, Department of Neurology, Boston Children’s Hospital, Harvard Medical School, Boston, MA, USACorrespondence[email protected]
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Hongwei Weia Genetic and Metabolic Central Laboratory, The Maternal and Child Health Care Hospital of Guangxi Zhuang Autonomous Region, Guangxi Birth Defects Prevention and Control Institute, Nanning, PR ChinaCorrespondence[email protected]
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Pages 2710-2716 | Received 09 Sep 2020, Accepted 17 Mar 2021, Published online: 02 May 2021

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