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