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Prenatal Diagnosis|February 15, 2022
Prenatal hydronephrosis: Bridging pre- and postnatal managementMandy Rickard, Joana Dos Santos, Johannes Keunen, et al.
Prenatal Diagnosis|September 27, 2021
Cell-free DNA screening for fetal aneuploidy using the rolling circle method: A step towards non invasive prenatal testing simplificationEnza Pavanello, Andrea Sciarrone, Varvara Guaraldo, et al.
Prenatal Diagnosis|February 8, 2022
Parental motivations for and adaptation to trio-exome sequencing in a prospective prenatal testing cohort: Beyond the diagnosisAsha N Talati, Kelly L Gilmore, Emily E Hardisty, et al.
Prenatal Diagnosis|February 1, 2022
Heterotaxy syndrome: Prenatal diagnosis, concomitant malformations and outcomesMünip Akalın, Oya Demirci, Pınar Kumru, et al.
Prenatal Diagnosis|June 21, 2019
Prognosis of fetuses with ventriculomegaly: An observational retrospective studyQingxian Chang, Yixian Peng, Qitao Huang, et al.
Prenatal Diagnosis|June 21, 2019
PREFACE: In silico pipeline for accurate cell-free fetal DNA fraction predictionLennart Raman, Machteld Baetens, Matthias De Smet, et al.
Prenatal Diagnosis|June 7, 2019
Analysis of PGT-M and PGT-SR outcomes at a Canadian fertility clinicRachel Butler, Gary Nakhuda, Colleen Guimond, et al.
Prenatal Diagnosis|June 7, 2019
Fetal pleural effusion: Contemporary methods of genetic evaluationTal Weissbach, Anya Kushnir, Rana Rasslan, et al.
Prenatal Diagnosis|June 5, 2019
Pandora's pregnancy: NIPT, CMA, and genome sequencing-A new era for prenatal genetic testingYael Hashiloni-Dolev, Tamar Nov-Klaiman, Aviad Raz
Prenatal Diagnosis|June 8, 2019
Prenatal findings in 1p36 deletion syndrome: New cases and a literature reviewSarah Guterman, Claire Beneteau, Sylvia Redon, et al.
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