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

dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T01:56:27Z
dc.date.available2014-05-27T01:56:27Z
dc.date.created2014-05-27T01:56:27Z
dc.date.issued1986-12-01
dc.identifierAmerican journal of medical genetics. Supplement, v. 2, p. 247-254.
dc.identifier1040-3787
dc.identifierhttp://hdl.handle.net/11449/63775
dc.identifier10.1002/ajmg.1320250628
dc.identifier2-s2.0-0022946119
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.
dc.languageeng
dc.relationAmerican journal of medical genetics. Supplement
dc.rightsAcesso restrito
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.
dc.typeArtículos de revistas


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