Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/2540
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dc.contributor.authorCuturilo, Goranen_US
dc.contributor.authorDrakulic, Danijelaen_US
dc.contributor.authorStevanović, Milenaen_US
dc.contributor.authorJovanovic, Idaen_US
dc.contributor.authorDjukic, Milanen_US
dc.contributor.authorMiletic-Grkovic, Slobodankaen_US
dc.contributor.authorAtanaskovic-Markovic, Marinaen_US
dc.date.accessioned2019-10-24T17:15:53Z-
dc.date.available2019-10-24T17:15:53Z-
dc.date.issued2008-10-
dc.identifier.issn0340-6199-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/2540-
dc.description.abstractMicrodeletion 22q11.2 is associated with a variety of findings, and the most common are cardiac defects. It is very frequently associated with interrupted aortic arch (IAA) type B and very rarely with type A and type C. Here we report the first case of IAA type C associated with 22q11.2 deletion in Serbia and, to the best of our knowledge, the fourth case described worldwide so far. By this report we would like to point out that all patients with IAA type C who have additional features specific for 22q11.2 microdeletion syndrome should be screened for the presence of this deletion. © 2007 Springer-Verlag.en_US
dc.language.isoenen_US
dc.relation.ispartofEuropean Journal of Pediatricsen_US
dc.subjectInterrupted aortic arch type Cen_US
dc.subjectMicrodeletion in chromosome 22q11.2en_US
dc.titleA rare association of interrupted aortic arch type C and microdeletion 22q11.2en_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s00431-007-0632-7-
dc.identifier.pmid18040716-
dc.identifier.scopus2-s2.0-50249181672-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/50249181672-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.grantfulltextrestricted-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.orcid0000-0003-4286-7334-
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