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dc.contributor.authorMorris, Joan K.
dc.contributor.authorBergman, Jorieke E. H.
dc.contributor.authorBarisic, Ingeborg
dc.contributor.authorWellesley, Diana
dc.contributor.authorTucker, David
dc.contributor.authorLimb, Elizabeth
dc.contributor.authorAddor, Marie-Claude
dc.contributor.authorCavero-Carbonell, Clara
dc.contributor.authorMatias Dias, Carlos
dc.contributor.authorDraper, Elisabeth S.
dc.contributor.authorEchevarría-González-de-Garibay, Luis Javier
dc.contributor.authorGatt, Miriam
dc.contributor.authorKlungsøyr, Kari
dc.contributor.authorLelong, Nathalie
dc.contributor.authorLuyt, Karen
dc.contributor.authorMaterna-Kiryluk, Anna
dc.contributor.authorNelen, Vera
dc.contributor.authorNeville, Amanda
dc.contributor.authorPerthus, Isabelle
dc.contributor.authorPierini, Anna
dc.contributor.authorRandrianaivo-Ranjatoelina, Hanitra
dc.contributor.authorRankin, Judith
dc.contributor.authorRissmann, Anke
dc.contributor.authorRouget, Florence
dc.contributor.authorSayers, Geraldine
dc.contributor.authorWertelecki, Wladimir
dc.contributor.authorKinsner-Ovaskainen, Agnieszka
dc.contributor.authorGarne, Ester
dc.date.accessioned2024-02-20T17:45:50Z
dc.date.available2024-02-20T17:45:50Z
dc.date.created2023-12-19T13:26:44Z
dc.date.issued2023
dc.identifier.citationEuropean Journal of Human Genetics. 2023, .
dc.identifier.issn1018-4813
dc.identifier.urihttps://hdl.handle.net/11250/3118789
dc.language.isoeng
dc.titleSurveillance of multiple congenital anomalies; searching for new associations
dc.title.alternativeSurveillance of multiple congenital anomalies; searching for new associations
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersion
dc.source.pagenumber0
dc.source.journalEuropean Journal of Human Genetics
dc.identifier.doi10.1038/s41431-023-01502-w
dc.identifier.cristin2215601
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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