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Prenatal Diagnosis|March 14, 2018
Diagnostic accuracy and clinical outcomes associated with prenatal diagnosis of fetal absent cavum septi pellucidiRachel A Pilliod, David R Pettersson, Thomas Gibson, et al.Prenatal Diagnosis|June 19, 2016
MCDA twins with discordant malformations: submicroscopic chromosomal anomalies detected by chromosomal microarray analysis and clinical outcomesRuan Peng, Yi Zhou, Hong-Ning Xie, et al.Prenatal Diagnosis|June 23, 2016
The benefits and limitations of cell-free DNA screening for 22q11.2 deletion syndromeLorraine Dugoff, Michael T Mennuti, Donna M McDonald-McGinnPrenatal Diagnosis|November 23, 2017
Should embryos with autosomal monosomy by preimplantation genetic testing for aneuploidy be transferred?: Implications for embryo selection from a systematic literature review of autosomal monosomy survivorsM E Bunnell, L Wilkins-Haug, R ReissPrenatal Diagnosis|January 23, 2023
Prenatal diagnosis of vascular anomaliesShreya Agarwal, Amy Mehollin-Ray, Vernon R Sutton, et al.Prenatal Diagnosis|January 23, 2023
Diagnostic yield and psychological outcomes among women pursuing trio-exome sequencing: Do women with recurrent anomalous fetal phenotypes experience more negative psychological outcomes?Asha N Talati, Kelly L Gilmore, Emily E Hardisty, et al.Prenatal Diagnosis|January 20, 2023
Fetal agenesis of the septum pellucidum: Ultrasonic diagnosis and clinical significanceXueyi Hu, Ning ShangPrenatal Diagnosis|January 12, 2002
Split notochord syndrome - prenatal ultrasonographic diagnosisB Almog, L Leibovitch, R AchironPrenatal Diagnosis|January 12, 2002
Minor sonographic signs of trisomy 21 at 15-20 weeks' gestation in fetuses born without malformations: a prospective studyE Viora, G Errante, S Bastonero, et al.Prenatal Diagnosis|December 18, 2001
Fetal and maternal progenitor cells in co-culture respond equally to erythropoietinR M Bohmer, K L Johnson, D W BianchiPageof 699