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Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases
Authors:Ioannis Papoulidis  Alexandros Sotiriadis  Elisavet Siomou  Elena Papageorgiou  Makarios Eleftheriades  Vasilios Papadopoulos  Eirini Oikonomidou  Sandro Orru  Emmanouil Manolakos  Apostolos Athanasiadis
Institution:1. Second Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, Thessaloniki, Greece;2. Access To Genome – ATG P.C., Thessaloniki, Greece;3. EMBRYOCARE Fetal Medicine Center, Athens, Greece;4. Department of Obstetrics and Gynecology, University of Patras Medical School, Patras, Greece;5. EuroGenetica S.A., Thessaloniki, Greece;6. Department of Medical Genetics, Cagliari University, Binaghi Hospital, Cagliari, Italy;7. First Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, Thessaloniki, Greece
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