Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleCell‐based noninvasive prenatal testing (cbNIPT) detects pathogenic copy number variations.AuthorsHatt, Lotte; Singh, Ripudaman; Christensen, Rikke; Ravn, Katarina; Christensen, Inga B; Jeppesen, Line Dahl; Nicolaisen, Bolette Hestbek; Kølvraa, Mathias; Schelde, Palle; Andreassen, Lotte; Farlie, Richard; Uldbjerg, Niels; Vogel, IdaAbstractIn two cases, cell‐based noninvasive prenatal testing (cbNIPT) detected pathogenic copy number variations (CNVs) in the fetal genome. cbNIPT may potentially be an improved noninvasive alternative for the detection of smaller CNVs.SubjectsPRENATAL diagnosis; PRADER-Willi syndromePublicationClinical Case Reports, 2020, Vol 8, Issue 12, p2561ISSN2050-0904Publication typeArticleDOI10.1002/ccr3.3211