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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/35532
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dc.contributor.authorGuionalmeida, M. L.-
dc.contributor.authorRodini, ESO-
dc.date.accessioned2014-05-20T15:25:03Z-
dc.date.accessioned2016-10-25T17:59:24Z-
dc.date.available2014-05-20T15:25:03Z-
dc.date.available2016-10-25T17:59:24Z-
dc.date.issued1995-07-03-
dc.identifierhttp://dx.doi.org/10.1002/ajmg.1320570302-
dc.identifier.citationAmerican Journal of Medical Genetics. New York: Wiley-liss, v. 57, n. 3, p. 377-379, 1995.-
dc.identifier.issn0148-7299-
dc.identifier.urihttp://hdl.handle.net/11449/35532-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/35532-
dc.description.abstractWe report on a Brazilian girl born to consanguineous parents and presenting with craniosynostosis, telecanthus, blepharophimosis, blepharoptosis, epicanthus inversus, cleft lip and palate, skeletal defects, and hearing loss. This combination of anomalies appears to constitute the Michels syndrome. (C) 1995 Wiley-Liss, Inc.en
dc.format.extent377-379-
dc.language.isoeng-
dc.publisherWiley-Blackwell-
dc.sourceWeb of Science-
dc.subjectCRANIOSYNOSTOSISpt
dc.subjectEYELID ABNORMALITIESpt
dc.subjectHYPERTELORISMpt
dc.subjectCLEFTINGpt
dc.subjectMICHELS SYNDROMEpt
dc.titleMICHELS SYNDROME IN A BRAZILIAN GIRL BORN TO CONSANGUINEOUS PARENTSen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUNIV ESTADUAL PAULISTA JULIO DE MESQUITA FILHO,FAC CIENCIAS,DEPT CIENCIAS BIOL,BAURU,SP,BRAZIL-
dc.description.affiliationUnespUNIV ESTADUAL PAULISTA JULIO DE MESQUITA FILHO,FAC CIENCIAS,DEPT CIENCIAS BIOL,BAURU,SP,BRAZIL-
dc.identifier.doi10.1002/ajmg.1320570302-
dc.identifier.wosWOS:A1995RF08300001-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofAmerican Journal of Medical Genetics-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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