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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.date.accessioned2022-11-22T22:01:03Z
dc.date.available2022-11-22T22:01:03Z
dc.date.issued2022-10-18
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.issn0197-3851
dc.identifier.otherPURE: 222275747
dc.identifier.otherPURE UUID: f8eedce6-f93e-47fe-8184-3cf5a83df3b9
dc.identifier.otherScopus: 85138557534
dc.identifier.otherPubMed: 36068932
dc.identifier.urihttps://hdl.handle.net/2164/19590
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.format.extent9
dc.language.isoeng
dc.relation.ispartofPrenatal Diagnosisen
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.https://creativecommons.org/licenses/by/4.0/en
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
dc.contributor.institutionUniversity of Aberdeen.Other Applied Health Sciencesen
dc.description.statusPeer revieweden
dc.description.versionPublisher PDFen
dc.identifier.doihttps://doi.org/10.1002/pd.6233
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85138557534&partnerID=8YFLogxKen
dc.identifier.vol42en
dc.identifier.iss11en


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