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Please use this identifier to cite or link to this item: http://sgc.anlis.gob.ar/handle/123456789/2437
DC FieldValueLanguage
dc.contributor.authorBell, Jane Ces
dc.contributor.authorBaynam, Garethes
dc.contributor.authorBergman, Jorieke E Hes
dc.contributor.authorBermejo-Sánchez, Evaes
dc.contributor.authorBotto, Lorenzo Des
dc.contributor.authorCanfield, Mark Aes
dc.contributor.authorDastgiri, Saeedes
dc.contributor.authorGatt, Miriames
dc.contributor.authorGroisman, Borises
dc.contributor.authorHurtado-Villa, Paulaes
dc.contributor.authorKällén, Karines
dc.contributor.authorKhoshnood, Babakes
dc.contributor.authorKonrad, Victoriaes
dc.contributor.authorLandau, Daniellees
dc.contributor.authorLópez Camelo, Jorgees
dc.contributor.authorMartinez, Lauraes
dc.contributor.authorMorgan, Margeryes
dc.contributor.authorMutchinick, Osvaldo Mes
dc.contributor.authorNance, Amy Ees
dc.contributor.authorNembhard, Wendy Nes
dc.contributor.authorPierini, Annaes
dc.contributor.authorRissmann, Ankees
dc.contributor.authorShan, Xiaoyies
dc.contributor.authorSipek, Antonines
dc.contributor.authorSzabova, Elenaes
dc.contributor.authorTagliabue, Giovannaes
dc.contributor.authorYevtushok, Lyubov Ses
dc.contributor.authorZarante, Ignacioes
dc.contributor.authorNassar, Natashaes
dc.date.accessioned2022-07-15T14:34:40Z-
dc.date.available2022-07-15T14:34:40Z-
dc.date.issued2021-
dc.identifier.urihttp://sgc.anlis.gob.ar/handle/123456789/2437-
dc.description.abstractEsophageal atresia (EA) affects around 2.3-2.6 per 10,000 births world-wide. Infants born with this condition require surgical correction soon after birth. Most survival studies of infants with EA are locally or regionally based. We aimed to describe survival across multiple world regions.es
dc.language.isoenes
dc.relation.ispartofBirth defects researches
dc.relation.ispartofseriesBirth defects research;Jul;12(4):219-233-
dc.subjectMortalidades
dc.subjectAberraciones Cromosómicases
dc.subjectEsophageal Atresiaes
dc.titleSurvival of infants born with esophageal atresia among 24 international birth defects surveillance programses
dc.typeArtículoes
dc.identifier.doi10.1002/bdr2.1891-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeArtículo-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptCentro Nacional de Genética Médica (CeNaGeM)-
crisitem.author.deptRegistro Nacional de Anomalías Congénitas (RENAC)-
crisitem.author.parentorgAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
crisitem.author.parentorgInstituto Nacional de Epidemiología (INE)-
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