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MICHELS SYNDROME IN A BRAZILIAN GIRL BORN TO CONSANGUINEOUS PARENTS

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dc.contributor.authorGuionalmeida, M. L.
dc.contributor.authorRodini, ESO
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:25:03Z
dc.date.available2014-05-20T15:25:03Z
dc.date.issued1995-07-03
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.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.format.extent377-379
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.doi10.1002/ajmg.1320570302
dc.identifier.issn0148-7299
dc.identifier.urihttp://hdl.handle.net/11449/35532
dc.identifier.wosWOS:A1995RF08300001
dc.language.isoeng
dc.publisherWiley-Blackwell
dc.relation.ispartofAmerican Journal of Medical Genetics
dc.rights.accessRightsAcesso restrito
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.typeArtigo
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dcterms.rightsHolderWiley-Blackwell
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências, Baurupt
unesp.departmentCiências Biológicas - FCpt

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Bauru - FC - Faculdade de Ciências