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Cell-free DNA screening for rare autosomal trisomies and segmental chromosome imbalances

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dc.contributor.authorRaymond, Yvette C.
dc.contributor.authorFernando, Shavi
dc.contributor.authorMenezes, Melody
dc.contributor.authorMeagher, Simon
dc.contributor.authorMol, Ben W.
dc.contributor.authorMcLennan, Andrew
dc.contributor.authorScott, Fergus
dc.contributor.authorMizia, Karen
dc.contributor.authorCarey, Karen
dc.contributor.authorFleming, Gabrielle
dc.contributor.authorRolnik, Daniel Lorber
dc.contributor.institutionUniversity of Aberdeen.Other Applied Health Sciencesen
dc.contributor.institutionUniversity of Aberdeen.Aberdeen Centre for Women’s Health Researchen
dc.date.accessioned2022-11-22T22:01:03Z
dc.date.available2022-11-22T22:01:03Z
dc.date.issued2022-10-18
dc.descriptionFunding 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.en
dc.description.statusPeer revieweden
dc.format.extent9
dc.format.extent466346
dc.identifier222275747
dc.identifierf8eedce6-f93e-47fe-8184-3cf5a83df3b9
dc.identifier85138557534
dc.identifier36068932
dc.identifier.citationRaymond, 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.6233en
dc.identifier.doi10.1002/pd.6233
dc.identifier.iss11en
dc.identifier.issn0197-3851
dc.identifier.urihttps://hdl.handle.net/2164/19590
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85138557534&partnerID=8YFLogxKen
dc.identifier.vol42en
dc.language.isoeng
dc.relation.ispartofPrenatal Diagnosisen
dc.subjectR Medicineen
dc.subjectObstetrics and Gynaecologyen
dc.subjectGenetics(clinical)en
dc.subject.lccRen
dc.titleCell-free DNA screening for rare autosomal trisomies and segmental chromosome imbalancesen
dc.typeJournal articleen

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