You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/63775
Full metadata record
DC FieldValueLanguage
dc.contributor.authorRichieri-Costa, A.-
dc.date.accessioned2014-05-27T01:56:27Z-
dc.date.accessioned2016-10-25T18:12:07Z-
dc.date.available2014-05-27T01:56:27Z-
dc.date.available2016-10-25T18:12:07Z-
dc.date.issued1986-12-01-
dc.identifierhttp://dx.doi.org/10.1002/ajmg.1320250628-
dc.identifier.citationAmerican journal of medical genetics. Supplement, v. 2, p. 247-254.-
dc.identifier.issn1040-3787-
dc.identifier.urihttp://hdl.handle.net/11449/63775-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/63775-
dc.description.abstractWe report on a Brazilian child with typical manifestations of the FG syndrome. Pigmentary dysplasia, metacarpal fusion and peculiar anatomopathological findings are additional undescribed signs.en
dc.format.extent247-254-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectBrazil-
dc.subjectcase report-
dc.subjectdermatoglyphics-
dc.subjecthuman-
dc.subjectmale-
dc.subjectmultiple malformation syndrome-
dc.subjectpreschool child-
dc.subjectradiography-
dc.subjectsyndrome-
dc.subjectAbnormalities, Multiple-
dc.subjectCase Report-
dc.subjectChild, Preschool-
dc.subjectDermatoglyphics-
dc.subjectHuman-
dc.subjectMale-
dc.subjectSupport, Non-U.S. Gov't-
dc.subjectSyndrome-
dc.titleFG syndrome in a Brazilian child with additional previously unreported signs.en
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.identifier.doi10.1002/ajmg.1320250628-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofAmerican journal of medical genetics. Supplement-
dc.identifier.scopus2-s2.0-0022946119-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
Show simple item record Show full item record   View Statistics
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.