FG syndrome in a Brazilian child with additional previously unreported signs.

dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorRichieri-Costa, A.
dc.date2014-05-27T01:56:27Z
dc.date2016-10-25T18:12:07Z
dc.date2014-05-27T01:56:27Z
dc.date2016-10-25T18:12:07Z
dc.date1986-12-01
dc.date.accessioned2017-04-06T00:40:53Z
dc.date.available2017-04-06T00:40:53Z
dc.identifierAmerican journal of medical genetics. Supplement, v. 2, p. 247-254.
dc.identifier1040-3787
dc.identifierhttp://hdl.handle.net/11449/63775
dc.identifierhttp://acervodigital.unesp.br/handle/11449/63775
dc.identifier10.1002/ajmg.1320250628
dc.identifier2-s2.0-0022946119
dc.identifierhttp://dx.doi.org/10.1002/ajmg.1320250628
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/885746
dc.descriptionWe report on a Brazilian child with typical manifestations of the FG syndrome. Pigmentary dysplasia, metacarpal fusion and peculiar anatomopathological findings are additional undescribed signs.
dc.languageeng
dc.relationAmerican journal of medical genetics. Supplement
dc.rightsinfo:eu-repo/semantics/closedAccess
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.
dc.typeOtro


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