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Expert Review of Molecular Diagnostics Volume 21, 2021 - Issue 4
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Review

Noninvasive prenatal screening for fetal sex chromosome aneuploidies

Cechuan Denga Medical Genetics Department/Prenatal Diagnostic Center, West China Second University Hospital, Sichuan University, Chengdu, China;b Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, ChinaORCID Iconhttps://orcid.org/0000-0002-8511-7990View further author information
ORCID Icon,
Sau Wai Cheungc Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USAORCID Iconhttps://orcid.org/0000-0002-3813-5256View further author information
ORCID Icon &
Hongqian Liua Medical Genetics Department/Prenatal Diagnostic Center, West China Second University Hospital, Sichuan University, Chengdu, China;b Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, ChinaCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0002-5229-793XView further author information
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Pages 405-415 | Received 21 Nov 2020, Accepted 30 Mar 2021, Published online: 11 Apr 2021

Citations (8)

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Read on this site (2)

Meng Tian, Lei Feng, Jinming Li & Rui Zhang. (2023) Focus on the frontier issue: progress in noninvasive prenatal screening for fetal trisomy from clinical perspectives. Critical Reviews in Clinical Laboratory Sciences 60:4, pages 248-269.
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Hilary Bowman-Smart, Christopher Gyngell, Cara Mand, David J. Amor, Martin B. Delatycki & Julian Savulescu. (2023) Non-Invasive Prenatal Testing for “Non-Medical” Traits: Ensuring Consistency in Ethical Decision-Making. The American Journal of Bioethics 23:3, pages 3-20.
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Articles from other publishers (6)

Sofia Bussolaro, Yvette C. Raymond, Melissa L. Acreman, Maurizio Guido, Fabricio Da Silva Costa, Daniel L. Rolnik & Ilaria Fantasia. (2023) The accuracy of prenatal cell-free DNA screening for sex chromosome abnormalities: A systematic review and meta-analysis. American Journal of Obstetrics & Gynecology MFM 5:3, pages 100844.
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Xinning Chen, Dan Lin, Yinghui Ye, Xiaohui Zhang & Danqing Chen. (2022) Trends in the prevalence, prenatal diagnosis, and outcomes of births with chromosomal abnormalities: a hospital-based study in Zhejiang Province, China during 2014–2020. Orphanet Journal of Rare Diseases 17:1.
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Haiwei Wang, Bin Liang, Yan Wang, Hailong Huang, Na Lin & Liangpu Xu. (2022) Retrospective analysis of the sex chromosomal copy number variations in 186 fetuses using single nucleotide polymorphism arrays. Frontiers in Genetics 13.
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Tazim Dowlut-McElroy, Shanlee Davis, Susan Howell, Iris Gutmark-Little, Vaneeta Bamba, Siddharth Prakash, Sheetal Patel, Doris Fadoju, Nandini Vijayakanthi, Mary Haag, Deborrah Hennerich, Lorraine Dugoff & Roopa Kanakatti Shankar. (2022) Cell-free DNA screening positive for monosomy X: clinical evaluation and management of suspected maternal or fetal Turner syndrome. American Journal of Obstetrics and Gynecology 227:6, pages 862-870.
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Yisheng Chen, Loukaiyi Lu, Ying Zhang, Feifei Wang, Yinghua Ni, Qiang Wang & Chunmei Ying. (2022) Clinical application of expanded noninvasive prenatal testing for fetal chromosome abnormalities in a cohort of 39,580 pregnancies. American Journal of Medical Genetics Part A 188:5, pages 1426-1434.
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Ganye Zhao, Peng Dai, Conghui Wang, Lina Liu, Xuechao Zhao & Xiangdong Kong. (2022) Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China. Frontiers in Medicine 8.
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