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Prenatal Diagnosis|August 24, 2016
Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representativesElizabeth Quinlan-Jones, Mark D Kilby, Sheila Greenfield, et al.Prenatal Diagnosis|July 8, 2017
Expanded carrier screening for monogenic disorders: where are we now?Davit Chokoshvili, Danya Vears, Pascal BorryPrenatal Diagnosis|June 28, 2017
Promises, pitfalls and practicalities of prenatal whole exome sequencingSunayna Best, Karen Wou, Neeta Vora, et al.Prenatal Diagnosis|June 29, 2017
Prenatal incision of ureterocele causing bladder outlet obstruction: a multicenter case seriesGihad E Chalouhi, Anne-Maude Morency, Roland De Vlieger, et al.Prenatal Diagnosis|March 17, 2010
Aortic isthmus Doppler velocimetry: role in assessment of preterm fetal growth restrictionM M Kennelly, N Farah, M J Turner, et al.Prenatal Diagnosis|February 2, 2010
Non-invasive detection and quantification of human foetal brain lactate in utero by magnetic resonance spectroscopyGeoffrey D Charles-Edwards, Wajanat Jan, Meekai To, et al.Prenatal Diagnosis|January 1, 1991
Extraction of DNA from amniotic fluid cells for the early prenatal diagnosis of genetic diseaseM T Rebello, G Hackett, J Smith, et al.Prenatal Diagnosis|January 1, 1991
The impact of supportive intervention after second trimester termination of pregnancy for fetal abnormalityS H Elder, K M LaurencePrenatal Diagnosis|June 3, 2018
The third ventricle of the human fetal brain: Normative data and pathologic correlation. A 3D transvaginal neurosonography studyRoee Birnbaum, Stefano Parodi, Gloria Donarini, et al.Prenatal Diagnosis|June 28, 2018
Fetal cerebral hemorrhage due to X-linked GATA1 gene mutationHanane Bouchghoul, Chloé Quelin, Philippe Loget, et al.Pageof 699