MICHELS SYNDROME IN A BRAZILIAN GIRL BORN TO CONSANGUINEOUS PARENTS

dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:25:03Z
dc.date.available2014-05-20T15:25:03Z
dc.date.created2014-05-20T15:25:03Z
dc.date.issued1995-07-03
dc.identifierAmerican Journal of Medical Genetics. New York: Wiley-liss, v. 57, n. 3, p. 377-379, 1995.
dc.identifier0148-7299
dc.identifierhttp://hdl.handle.net/11449/35532
dc.identifier10.1002/ajmg.1320570302
dc.identifierWOS:A1995RF08300001
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.
dc.languageeng
dc.publisherWiley-Blackwell
dc.relationAmerican Journal of Medical Genetics
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectCRANIOSYNOSTOSIS
dc.subjectEYELID ABNORMALITIES
dc.subjectHYPERTELORISM
dc.subjectCLEFTING
dc.subjectMICHELS SYNDROME
dc.titleMICHELS SYNDROME IN A BRAZILIAN GIRL BORN TO CONSANGUINEOUS PARENTS
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución