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Survival of children with rare structural congenital anomalies: a multi-registry cohort study

dc.contributor.authorCoi, Alessio
dc.contributor.authorSantoro, Michele
dc.contributor.authorPierini, Anna
dc.contributor.authorRankin, Judith
dc.contributor.authorGlinianaia, Svetlana V.
dc.contributor.authorTan, Joachim
dc.contributor.authorReid, Abigail-Kate
dc.contributor.authorGarne, Ester
dc.contributor.authorLoane, Maria
dc.contributor.authorGiven, Joanne
dc.contributor.authorBallardini, Elisa
dc.contributor.authorCavero-Carbonell, Clara
dc.contributor.authorde Walle, Hermien E.K.
dc.contributor.authorGatt, Miriam
dc.contributor.authorGarcía-Villodre, Laura
dc.contributor.authorGissler, Mika
dc.contributor.authorJordan, Sue
dc.contributor.authorKiuru-Kuhlefelt, Sonja
dc.contributor.authorKjaer Urhoj, Stine
dc.contributor.authorKlungsøyr, Kari
dc.contributor.authorLelong, Nathalie
dc.contributor.authorLutke, L. Renée
dc.contributor.authorNeville, Amanda J.
dc.contributor.authorRahshenas, Makan
dc.contributor.authorScanlon, Ieuan
dc.contributor.authorWellesley, Diana
dc.contributor.authorMorris, Joan K.
dc.date.accessioned2022-07-29T07:08:01Z
dc.date.available2022-07-29T07:08:01Z
dc.date.created2022-05-28T13:53:04Z
dc.date.issued2022
dc.identifier.citationOrphanet Journal of Rare Diseases. 2022, 17 1-11.
dc.identifier.issn1750-1172
dc.identifier.urihttps://hdl.handle.net/11250/3009090
dc.language.isoeng
dc.titleSurvival of children with rare structural congenital anomalies: a multi-registry cohort study
dc.title.alternativeSurvival of children with rare structural congenital anomalies: a multi-registry cohort study
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersion
dc.source.pagenumber1-11
dc.source.volume17
dc.source.journalOrphanet Journal of Rare Diseases
dc.identifier.doi10.1186/s13023-022-02292-y
dc.identifier.cristin2027879
dc.relation.projectEC/H2020/733001
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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