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Original Research

Amniocentesis and Next Generation Sequencing (NGS)-Based Noninvasive Prenatal DNA Testing (NIPT) for Prenatal Diagnosis of Fetal Chromosomal Disorders

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Pages 1811-1817 | Published online: 11 May 2021

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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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Articles from other publishers (4)

Priyanka Jha, Preethi Raghu, Anne M. Kennedy, Mark Sugi, Tara A. Morgan, Vickie Feldstein, Liina Pōder & Rubal Penna. (2023) Assessment of Amniotic Fluid Volume in Pregnancy. RadioGraphics 43:6.
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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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Zachary Demko, Brittany Prigmore & Peter Benn. (2022) A Critical Evaluation of Validation and Clinical Experience Studies in Non-Invasive Prenatal Testing for Trisomies 21, 18, and 13 and Monosomy X. Journal of Clinical Medicine 11:16, pages 4760.
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Zhenglong Guo, Bing Kang, Dong Wu, Hai Xiao, Leilei Hao, Bingtao Hao & Shixiu Liao. (2022) Case Report: Twin Pregnancy Gives Birth to a Girl with Partial Trisomy 21 Mosaicism after in vitro Fertilization and Embryo Transfer. Frontiers in Genetics 12.
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