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Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth

dc.contributor.authorHuusko, Johanna M
dc.contributor.authorKarjalainen, Minna K
dc.contributor.authorGraham, Britney E
dc.contributor.authorJacobsson, Bo
dc.contributor.authorMuglia, Louis J
dc.date.accessioned2018-08-06T10:38:23Z
dc.date.available2018-08-06T10:38:23Z
dc.date.created2018-08-01T13:17:09Z
dc.date.issued2018
dc.identifier.citationPLoS Genetics. 2018, 14 (7), .
dc.identifier.issn1553-7390
dc.identifier.urihttp://hdl.handle.net/11250/2507499
dc.language.isoeng
dc.relation.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6042692/pdf/pgen.1007394.pdf
dc.titleWhole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth
dc.title.alternativeWhole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersion
dc.source.pagenumber22
dc.source.volume14
dc.source.journalPLoS Genetics
dc.source.issue7
dc.identifier.doi10.1371/ journal.pgen.1007394
dc.identifier.cristin1599353
cristin.unitcode7502,5,2,0
cristin.unitnameGenetikk og bioinformatikk
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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