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Hailong Huang, Meiying Cai, Yan Wang, Bin Liang, Na Lin & Liangpu Xu. (2021) SNP Array as a Tool for Prenatal Diagnosis of Congenital Heart Disease Screened by Echocardiography: Implications for Precision Assessment of Fetal Prognosis. Risk Management and Healthcare Policy 14, pages 345-355.
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Jiping Shi, Runling Zhang, Jinming Li & Rui Zhang. (2019) Novel perspectives in fetal biomarker implementation for the noninvasive prenatal testing. Critical Reviews in Clinical Laboratory Sciences 56:6, pages 374-392.
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Articles from other publishers (28)
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Simon M. Outram, Julia E. H. Brown, Astrid N. Zamora, Nuriye Sahin-Hodoglugil & Sara L. Ackerman. (2022) Parental Hopes and Understandings of the Value of Prenatal Diagnostic Genomic Sequencing: A Qualitative Analysis. Frontiers in Genetics 13.
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Heinz Gabriel, Dirk Korinth, Martin Ritthaler, Björn Schulte, Florian Battke, Constantin von Kaisenberg, Max Wüstemann, Bernt Schulze, Almuth Friedrich‐Freksa, Lutz Pfeiffer, Michael Entezami, Andreas Schröer, Joachim Bürger, Eva Maria Christina Schwaibold, Holger Lebek & Saskia Biskup. (2021) Trio exome sequencing is highly relevant in prenatal diagnostics. Prenatal Diagnosis 42:7, pages 845-851.
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Dagmar Schmitz & Marcus Düwell. (2021) Die Rechte zukünftiger Kinder im Kontext pränataler DiagnostikThe rights of future children in the context of prenatal testing. Ethik in der Medizin 34:1, pages 49-63.
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Gioia Mastromoro, Daniele Guadagnolo, Nader Khaleghi Hashemian, Enrica Marchionni, Alice Traversa & Antonio Pizzuti. (2022) Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges—Systematic Review of the Literature and Meta-Analysis. Diagnostics 12:3, pages 575.
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Shuang Fei, Zeping Gui, Dengyuan Feng, Zijie Wang, Ming Zheng, Hao Chen, Li Sun, Jun Tao, Zhijian Han, Xiaobing Ju, Min Gu, Ruoyun Tan & Xinli Li. (2022) Association Between a TLR2 Gene Polymorphism (rs3804099) and Proteinuria in Kidney Transplantation Recipients. Frontiers in Genetics 12.
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Daniele Guadagnolo, Gioia Mastromoro, Francesca Di Palma, Antonio Pizzuti & Enrica Marchionni. (2021) Prenatal Exome Sequencing: Background, Current Practice and Future Perspectives—A Systematic Review. Diagnostics 11:2, pages 224.
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