Congenial heart disease revealing familial Velocardiofacial syndrome caused by 3 Mb deletion at 22q11 region

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dc.contributor.authorRibeiro-Bicudo, L. A.
dc.contributor.authorOliveira, C. C.
dc.contributor.authorGomes, T. G. [UNESP]
dc.contributor.authorSantos, M. V.
dc.contributor.authorBergamo, N. A.
dc.contributor.authorRocha, R. H.
dc.contributor.authorGamba, B. F.
dc.contributor.institutionUniversidade Federal de Goiás (UFG)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2020-12-10T16:57:45Z
dc.date.available2020-12-10T16:57:45Z
dc.date.issued2018-10-01
dc.description.affiliationUniv Fed Goias, Goiania, Go, Brazil
dc.description.affiliationUNESP, Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP, Botucatu, SP, Brazil
dc.format.extent962-962
dc.identifier.citationEuropean Journal Of Human Genetics. London: Nature Publishing Group, v. 26, p. 962-962, 2018.
dc.identifier.issn1018-4813
dc.identifier.urihttp://hdl.handle.net/11449/194889
dc.identifier.wosWOS:000489312608082
dc.language.isoeng
dc.publisherNature Publishing Group
dc.relation.ispartofEuropean Journal Of Human Genetics
dc.sourceWeb of Science
dc.titleCongenial heart disease revealing familial Velocardiofacial syndrome caused by 3 Mb deletion at 22q11 regionen
dc.typeResumo
dcterms.rightsHolderNature Publishing Group

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