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Authordc.contributor.authorCortés, 
Authordc.contributor.authorCurotto, 
Authordc.contributor.authorRios, Marco 
Authordc.contributor.authorBarrios, 
Authordc.contributor.authorAlliende, Isabel 
Admission datedc.date.accessioned2019-01-29T14:52:16Z
Available datedc.date.available2019-01-29T14:52:16Z
Publication datedc.date.issued1996
Cita de ítemdc.identifier.citationPediatric Research, Volumen 39, Issue 2, 2018,
Identifierdc.identifier.issn15300447
Identifierdc.identifier.issn00313998
Identifierdc.identifier.other10.1203/00006450-199602000-00037
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/161065
Lenguagedc.language.isoen
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourcePediatric Research
Keywordsdc.subjectPediatrics, Perinatology and Child Health
Títulodc.titleClinical and cytogenetical diagnosis in the fragil x syndrome
Document typedc.typeArtículo de revista
dcterms.accessRightsdcterms.accessRightsAcceso Abierto
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile