Clinical validation of a novel automated cell-free DNA screening assay for trisomies 21, 13, and 18 in maternal plasma
dc.contributor.author | Ericsson, Olle | |
dc.contributor.author | Ahola, Tarja | |
dc.contributor.author | Dahl, Fredrik | |
dc.contributor.author | Karlsson, Filip | |
dc.contributor.author | Persson, Fredrik | |
dc.contributor.author | Karlberg, Olof | |
dc.contributor.author | Roos, Fredrik | |
dc.contributor.author | Alftrén, Ida | |
dc.contributor.author | Andersson, Björn | |
dc.contributor.author | Barkenäs, Emelie | |
dc.contributor.author | Boghos, Ani | |
dc.contributor.author | Brandner, Birgit | |
dc.contributor.author | Dahlberg, Jenny | |
dc.contributor.author | Forsgren, Per-Ola | |
dc.contributor.author | Francois, Niels | |
dc.contributor.author | Gousseva, Anna | |
dc.contributor.author | Hakamali, Faizan | |
dc.contributor.author | Janfalk-Carlsson, Åsa | |
dc.contributor.author | Johansson, Henrik | |
dc.contributor.author | Lundgren, Johanna | |
dc.contributor.author | Mohsenchian, Atefeh | |
dc.contributor.author | Olausson, Linus | |
dc.contributor.author | Olofsson, Simon | |
dc.contributor.author | Qureshi, Atif | |
dc.contributor.author | Skarpås, Björn | |
dc.contributor.author | Svahn, Peter | |
dc.contributor.author | Sävneby, Anna | |
dc.contributor.author | Åström, Eva | |
dc.contributor.author | Sahlberg, Anna | |
dc.contributor.author | Fianu-Jonasson, Aino | |
dc.contributor.author | Gautier, Jérémie | |
dc.contributor.author | Costa, Jean-Marc | |
dc.contributor.author | Jacobsson, Bo | |
dc.contributor.author | Nicolaides, Kypros | |
dc.date.accessioned | 2020-02-20T09:06:05Z | |
dc.date.available | 2020-02-20T09:06:05Z | |
dc.date.created | 2019-11-21T13:02:01Z | |
dc.date.issued | 2019 | |
dc.identifier.citation | Prenatal Diagnosis. 2019, 39 1011-1015. | |
dc.identifier.issn | 0197-3851 | |
dc.identifier.uri | http://hdl.handle.net/11250/2642761 | |
dc.language.iso | eng | |
dc.title | Clinical validation of a novel automated cell-free DNA screening assay for trisomies 21, 13, and 18 in maternal plasma | |
dc.type | Peer reviewed | |
dc.type | Journal article | |
dc.description.version | publishedVersion | |
dc.source.pagenumber | 1011-1015 | |
dc.source.volume | 39 | |
dc.source.journal | Prenatal Diagnosis | |
dc.identifier.doi | 10.1002/pd.5528 | |
dc.identifier.cristin | 1750469 | |
cristin.unitcode | 7502,5,2,0 | |
cristin.unitname | Avdeling for genetikk og bioinformatikk | |
cristin.ispublished | true | |
cristin.fulltext | original | |
cristin.qualitycode | 1 |
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