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

dc.contributorUniversidade Federal de Goiás (UFG)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2020-12-10T16:57:45Z
dc.date.accessioned2022-12-19T19:57:46Z
dc.date.available2020-12-10T16:57:45Z
dc.date.available2022-12-19T19:57:46Z
dc.date.created2020-12-10T16:57:45Z
dc.date.issued2018-10-01
dc.identifierEuropean Journal Of Human Genetics. London: Nature Publishing Group, v. 26, p. 962-962, 2018.
dc.identifier1018-4813
dc.identifierhttp://hdl.handle.net/11449/194889
dc.identifierWOS:000489312608082
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5375526
dc.languageeng
dc.publisherNature Publishing Group
dc.relationEuropean Journal Of Human Genetics
dc.sourceWeb of Science
dc.titleCongenial heart disease revealing familial Velocardiofacial syndrome caused by 3 Mb deletion at 22q11 region
dc.typeOtros


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