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Prenatal Diagnosis|November 1, 1989
Missed prenatal diagnosis of fragile-X syndromeT P Webb, S Bundey, M McKinleyPrenatal Diagnosis|April 26, 2020
Rapid whole exome sequencing in pregnancies to identify the underlying genetic cause in fetuses with congenital anomalies detected by ultrasound imagingChantal Deden, Kornelia Neveling, Dimitra Zafeiropopoulou, et al.Prenatal Diagnosis|April 27, 2020
Medications for pregnant women: A balancing act between the interests of the mother and of the fetusNorman R Saunders, Katarzyna M DziegielewskaPrenatal Diagnosis|April 13, 2020
Is laterality of congenital diaphragmatic hernia a reliable prognostic factor? French national cohort studyAnne Pinton, Julia Boubnova, François Becmeur, et al.Prenatal Diagnosis|April 14, 2020
A review of fetal and neonatal consequences of maternal systemic lupus erythematosusMeghana A Limaye, Jill P Buyon, Bettina F Cuneo, et al.Prenatal Diagnosis|May 4, 2020
Neurodevelopmental impairment at 3 years of age after fetoscopic laser surgery for twin-to-twin transfusion syndromeSachio Matsushima, Katsusuke Ozawa, Rika Sugibayashi, et al.Prenatal Diagnosis|May 4, 2020
Congenital syphilis: A contemporary update on an ancient diseaseMartha W F Rac, Irene A Stafford, Catherine S EppesPrenatal Diagnosis|April 17, 2020
Recognizing the unique prenatal phenotype of Prader-Willi Syndrome (PWS) indicates the need for a diagnostic methylation testNaama Srebnik, Noa Gross Even-Zohar, Abdalla Salama, et al.Prenatal Diagnosis|April 12, 2020
Periventricular pseudocysts of noninfectious origin: Prenatal associated findings and prognostic factorsMichal Levy, Dorit Lev, Zvi Leibovitz, et al.Prenatal Diagnosis|August 1, 1992
Increased maternal serum alpha-fetoprotein and human chorionic gonadotropin in compromised pregnancies other than for neural tube defects or Down syndromeJ R Beekhuis, J M Van Lith, B T De Wolf, et al.Pageof 696