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Routine obstetrical ultrasound at 18-22 weeks: our experience on 7,236 fetuses.
Stefos T, Plachouras N, Sotiriadis A, Papadimitriou D, Almoussa N, Navrozoglou I, Lolis D. Stefos T, et al. Among authors: sotiriadis a. J Matern Fetal Med. 1999 Mar-Apr;8(2):64-9. doi: 10.1002/(SICI)1520-6661(199903/04)8:2<64::AID-MFM7>3.0.CO;2-D. J Matern Fetal Med. 1999. PMID: 10090494
Dual testing with QF-PCR and karyotype analysis for prenatal diagnosis of chromosomal abnormalities. Evaluation of 13,500 cases with consideration of using QF-PCR as a stand-alone test according to referral indications.
Papoulidis I, Siomou E, Sotiriadis A, Efstathiou G, Psara A, Sevastopoulou E, Anastasakis E, Sifakis S, Tsiligianni T, Kontodiou M, Malamaki C, Tzimina M, Petersen MB, Manolakos E, Athanasiadis A. Papoulidis I, et al. Among authors: sotiriadis a. Prenat Diagn. 2012 Jul;32(7):680-5. doi: 10.1002/pd.3888. Epub 2012 Apr 18. Prenat Diagn. 2012. PMID: 22513450
Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases.
Papoulidis I, Sotiriadis A, Siomou E, Papageorgiou E, Eleftheriades M, Papadopoulos V, Oikonomidou E, Orru S, Manolakos E, Athanasiadis A. Papoulidis I, et al. Among authors: sotiriadis a. Prenat Diagn. 2015 Dec;35(13):1269-77. doi: 10.1002/pd.4685. Epub 2015 Oct 26. Prenat Diagn. 2015. PMID: 26289927
183 results