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Prenatal Diagnosis|December 9, 2023
Precarious hope: Ethical considerations for offering experimental fetal therapies outside of research after initial studies in humansSaskia Hendriks, Janyne Althaus, Meredith A Atkinson, et al.Prenatal Diagnosis|December 9, 2023
Impact of high-risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART studyKimberly Martin, Mary E Norton, Cora MacPherson, et al.Prenatal Diagnosis|November 15, 2023
Congenital small bowel obstruction: Prenatal detection and outcomeH Heinrich, A G H Pijpers, I H Linskens, et al.Prenatal Diagnosis|November 17, 2023
Improving the accuracy of noninvasive prenatal testing through size-selection between fetal and maternal cfDNAHyuk-Jung Kwon, Seonyoung Yun, Joungsu Joo, et al.Prenatal Diagnosis|September 5, 2024
Potentially Missed Diagnoses in Prenatal Versus Postnatal Exome Sequencing in the Lack of Informative Phenotype: Lessons Learned From a Postnatal CohortDana Brabbing-Goldstein, Lily Bazak, Noa Ruhrman-Shahar, et al.Prenatal Diagnosis|September 4, 2024
Prenatal Phenotype of Alkuraya-Kučinskas Syndrome: A Novel Case and Systematic Literature ReviewStephanie M Rice, Dante F Varotsis, Sascha Wodoslawsky, et al.Prenatal Diagnosis|June 6, 2024
Associations and outcomes of prenatally detected rhombencephalosynapsisYada Kunpalin, Elka Miller, Kamini Raghuram, et al.Prenatal Diagnosis|July 11, 2024
Accuracy of fetal fraction measurements in a single-nucleotide polymorphism-based noninvasive prenatal testPeter Benn, Jingwen Zhang, Daniel Lyons, et al.Prenatal Diagnosis|May 16, 2024
Maternal "mirror" syndrome: Evaluating the benefits of fetal therapyJoanna Sichitiu, Fawaz Alkazaleh, Roel de Heus, et al.Prenatal Diagnosis|May 20, 2024
Truncating variants in PAPSS2 gene: A cause of early prenatal onset brachyolmia?Giulia Biancotto, Giulia Rosti, Francesca Madia, et al.Pageof 699