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Prenatal Diagnosis|December 27, 2021
Trio exome sequencing is highly relevant in prenatal diagnosticsHeinz Gabriel, Dirk Korinth, Martin Ritthaler, et al.
Prenatal Diagnosis|June 1, 1987
Karyotypic differences between cells from placenta and other fetal tissuesM Verjaal, N J Leschot, H Wolf, et al.
Prenatal Diagnosis|January 6, 2022
Impact of introducing cell-free DNA screening into clinical care on first trimester ultrasoundGeorgios Doulaveris, Catherine M Igel, Fatima Estrada Trejo, et al.
Prenatal Diagnosis|July 1, 2011
Fragile X analysis of 1112 prenatal samples from 1991 to 2010Sarah L Nolin, Anne Glicksman, Xiaohua Ding, et al.
Prenatal Diagnosis|June 4, 2011
Prenatal pharmacotherapy for fetal anomalies: a 2011 updateLisa Hui, Diana W Bianchi
Prenatal Diagnosis|June 28, 2011
Preventing mucopolysaccharidosis type II (Hunter syndrome): PGD and establishing a Hunter (46, XX) stem cell lineGheona Altarescu, Paul Renbaum, Talia Eldar-Geva, et al.
Prenatal Diagnosis|June 28, 2011
Effect of cord puncture site in cordocentesis at mid-pregnancy on pregnancy outcomesChayada Tangshewinsirikul, Chanane Wanapirak, Wirawit Piyamongkol, et al.
Prenatal Diagnosis|June 28, 2011
Ultrasound detection rate of single umbilical artery in the first trimester of pregnancyClarissa O Lamberty, Mário Henrique Burlacchini de Carvalho, Javier Miguelez, et al.
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