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Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents

dc.contributor.authorSmajlagic, Dinka
dc.contributor.authorLavrichenko, Ksenia
dc.contributor.authorBerland, Siren
dc.contributor.authorHelgeland, Øyvind
dc.contributor.authorKnudsen, Gun Peggy Strømstad
dc.contributor.authorVaudel, Marc
dc.contributor.authorHaavik, Jan
dc.contributor.authorKnappskog, Per
dc.contributor.authorNjølstad, Pål Rasmus
dc.contributor.authorHouge, Gunnar
dc.contributor.authorJohansson, Stefan
dc.date.accessioned2023-05-08T09:58:51Z
dc.date.available2023-05-08T09:58:51Z
dc.date.created2020-11-10T18:56:23Z
dc.date.issued2020
dc.identifier.citationEuropean Journal of Human Genetics. 2020, 29 205-215.
dc.identifier.issn1018-4813
dc.identifier.urihttps://hdl.handle.net/11250/3066734
dc.language.isoeng
dc.titlePopulation prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersion
dc.source.pagenumber205-215
dc.source.volume29
dc.source.journalEuropean Journal of Human Genetics
dc.identifier.doi10.1038/s41431-020-00707-7
dc.identifier.cristin1846702
dc.relation.projectERC-European Research Council: 293574
dc.relation.projectNovo Nordisk Fonden: NNF19OC0057445
dc.relation.projectNorges forskningsråd: 240413
dc.relation.projectNovo Nordisk Fonden: NNF19OC0054741
dc.relation.projectNorges forskningsråd: 229624
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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