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Prenatal Diagnosis|March 19, 2025
Can Fetal Heterotaxy Syndrome Be Diagnosed Through Prenatal Ultrasound in the First Trimester (GA 11+0-13+6 Weeks)?Biying Huang, Qiumei Wu, Shan Guo, et al.Prenatal Diagnosis|April 21, 1999
Clinical follow-up of high mid-trimester maternal serum intact human chorionic gonadotrophin concentrations in singleton pregnanciesG Blundell, J P Ashby, C Martin, et al.Prenatal Diagnosis|April 21, 1999
Fetal lactic dehydrogenase variation in normal pregnancy and in cases of severe intra-uterine growth restrictionE Verspyck, G Gaillard, F Parnet, et al.Prenatal Diagnosis|April 21, 1999
Amniocentesis or chorionic villus sampling in multiple gestations? Experience with 500 casesC van den Berg, A P Braat, D Van Opstal, et al.Prenatal Diagnosis|April 21, 1999
Trisomy 17 mosaicism in amniotic fluid cells not found at birth in blood but present in skin fibroblastsG Lesca, D Boggio, V Bellec, et al.Prenatal Diagnosis|April 21, 1999
Detection of fetal-specific DNA after enrichment for trophoblasts using the monoclonal antibody LK26 in model systems but failure to demonstrate fetal DNA in maternal peripheral bloodT V Hviid, S Sørensen, N MorlingPrenatal Diagnosis|April 21, 1999
Hydrolethalus syndrome in a non-Finnish family: confirmation of the entity and early prenatal diagnosisT J de Ravel, M C van der Griendt, P Evan, et al.Prenatal Diagnosis|October 15, 2003
Ethmocephaly caused by de novo translocation 18;21--prenatal diagnosisIsrael Goldstein, Amir Weissman, Ronit Brill-Zamir, et al.Prenatal Diagnosis|October 15, 2003
Prenatal diagnosis of capillary telangiectasia of the cerebellum--ultrasound and MRI featuresLaurent Guibaud, Catherine Garel, Buenerd Annie, et al.Prenatal Diagnosis|October 15, 2003
Cryptic 1p36.3/6q25.2 translocation in three generations ascertained through a foetus with IUGR and cerebral malformationsS Cavani, C Perfumo, F Faravelli, et al.Pageof 699