Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/42810
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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP
dc.contributor.authorZAMARIOLLI, M.
dc.contributor.authorDANTAS, A. G.
dc.contributor.authorNUNES, N.
dc.contributor.authorMOYSES-OLIVEIRA, M.
dc.contributor.authorSGARDIOLI, I. C.
dc.contributor.authorSOARES, D. C. Q.
dc.contributor.authorGIL-DA-SILVA-LOPES, V. L.
dc.contributor.authorKIM, C. A.
dc.contributor.authorMELARAGNO, M. I.
dc.date.accessioned2021-11-22T20:29:31Z-
dc.date.available2021-11-22T20:29:31Z-
dc.date.issued2020
dc.identifier.citationEUROPEAN JOURNAL OF HUMAN GENETICS, v.28, n.SUPPL 1, suppl.1, p.452-453, 2020
dc.identifier.issn1018-4813
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/42810-
dc.language.isoeng
dc.publisherSPRINGERNATUREeng
dc.relation.ispartofEuropean Journal of Human Genetics
dc.rightsrestrictedAccesseng
dc.titlePhenotypic heterogeneity in 22q11.2 deletion syndrome: CNVs as genetic modifiers for congenital heart disease in a Brazilian cohorteng
dc.typeconferenceObjecteng
dc.rights.holderCopyright SPRINGERNATUREeng
dc.subject.wosBiochemistry & Molecular Biologyeng
dc.subject.wosGenetics & Heredityeng
dc.type.categorymeeting abstracteng
dc.type.versionpublishedVersioneng
hcfmusp.author.externalZAMARIOLLI, M.:Univ Fed Sao Paulo, Sao Paulo, Brazil
hcfmusp.author.externalDANTAS, A. G.:Univ Fed Sao Paulo, Sao Paulo, Brazil
hcfmusp.author.externalNUNES, N.:Univ Fed Sao Paulo, Sao Paulo, Brazil
hcfmusp.author.externalMOYSES-OLIVEIRA, M.:Univ Fed Sao Paulo, Sao Paulo, Brazil
hcfmusp.author.externalSGARDIOLI, I. C.:Univ Estadual Campinas, Campinas, Brazil
hcfmusp.author.externalGIL-DA-SILVA-LOPES, V. L.:Univ Estadual Campinas, Campinas, Brazil
hcfmusp.author.externalMELARAGNO, M. I.:Univ Fed Sao Paulo, Sao Paulo, Brazil
hcfmusp.description.beginpage452
hcfmusp.description.endpage453
hcfmusp.description.issueSUPPL 1
hcfmusp.description.issuesuppl 1
hcfmusp.description.volume28
hcfmusp.origemWOS
hcfmusp.origem.idWOS:000598482601394
hcfmusp.publisher.cityLONDONeng
hcfmusp.publisher.countryENGLANDeng
dc.description.indexMEDLINEeng
dc.identifier.eissn1476-5438
Appears in Collections:

Comunicações em Eventos - FM/MPE
Departamento de Pediatria - FM/MPE

Comunicações em Eventos - LIM/03
LIM/03 - Laboratório de Medicina Laboratorial

Comunicações em Eventos - LIM/36
LIM/36 - Laboratório de Pediatria Clínica


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