All-in-one Whole Exome Sequencing Strategy with Simultaneous Copy Number Variant, Single Nucleotide Variant and Absence-of-heterozygosity Analysis in Fetuses with Structural Ultrasound Anomalies: A 1-Year ExperienceBrigitte H. W. Faas,Dineke Westra,Sonja A. de Munnik,Maartje van Rij,Carlo Marcelis, Sara Joosten,Ingrid Krapels,Vivian Vernimmen,Malou Heijligers,Marjolein H. Willemsen,Nicole de Leeuw,Tuula Rinne,Rolph Pfundt,Sanne P. Smeekens,Sander P. A. Stegmann,Merryn Macville,Esther Sikkel,Audrey Coumans,Lia Wijnberger,Irma Derks,Josefa van Lent-Albrechts,Tom Hofste,Raoul Timmermans,Janneke van den End,Servi J. C. Stevens,Ilse FeenstraPRENATAL DIAGNOSIS（2023）引用 0|浏览33AI 理解论文溯源树样例生成溯源树，研究论文发展脉络Chat Paper正在生成论文摘要
