MOESM3 of Targeted capture enrichment followed by NGS: development and validation of a single comprehensive NIPT for chromosomal aneuploidies, microdeletion syndromes and monogenic diseases George Koumbaris Achilleas Achilleos Michalis Nicolaou Charalambos Loizides Kyriakos Tsangaras Elena Kypri Petros Mina Carolina Sismani Voula Velissariou Georgia Christopoulou Pantelis Constantoulakis Emmanouil Manolakos Ioannis Papoulidis Danai Stambouli Marios Ioannides Philippos Patsalis 10.6084/m9.figshare.10730849.v1 https://springernature.figshare.com/articles/journal_contribution/MOESM3_of_Targeted_capture_enrichment_followed_by_NGS_development_and_validation_of_a_single_comprehensive_NIPT_for_chromosomal_aneuploidies_microdeletion_syndromes_and_monogenic_diseases/10730849 Additional file 3: Table S2. The theoretical and estimated risk for the parents and the fetus. 2019-11-22 05:59:17 NIPT Monogenic diseases Cell-free DNA Aneuploidies Microdeletions