Raymond, Yvette C.Fernando, ShaviMenezes, MelodyMeagher, SimonMol, Ben W.McLennan, AndrewScott, FergusMizia, KarenCarey, KarenFleming, GabrielleRolnik, Daniel Lorber2022-11-222022-11-222022-10-18Raymond, Y C, Fernando, S, Menezes, M, Meagher, S, Mol, B W, McLennan, A, Scott, F, Mizia, K, Carey, K, Fleming, G & Rolnik, D L 2022, 'Cell-free DNA screening for rare autosomal trisomies and segmental chromosome imbalances', Prenatal Diagnosis, vol. 42, no. 11, pp. 1349-1357. https://doi.org/10.1002/pd.62330197-3851https://hdl.handle.net/2164/19590Funding Information: Ben W. Mol is supported by a NHMRC Investigator grant (GNT1176437). Ben W. Mol reports consultancy for ObsEva and Merck and travel support and research grants from Merck. The authors declare no conflict of interest. The authors wish to acknowledge the staff of Monash Ultrasound for Women, Sydney Ultrasound for Women, and Ultrasound Care for their diligent and compassionate care of the women involved in this study. Open access publishing facilitated by Monash University, as part of the Wiley - Monash University agreement via the Council of Australian University Librarians.9466346engR MedicineObstetrics and GynaecologyGenetics(clinical)RJournal article10.1002/pd.6233http://www.scopus.com/inward/record.url?scp=85138557534&partnerID=8YFLogxK4211