dc.creatorFerraz, LFC
dc.creatorGuerra, G
dc.creatorBaptista, MTM
dc.creatorMaciel-Guerra, AT
dc.creatorHackel, C
dc.date1998
dc.dateMAY-JUN
dc.date2014-12-02T16:28:42Z
dc.date2015-11-26T16:37:54Z
dc.date2014-12-02T16:28:42Z
dc.date2015-11-26T16:37:54Z
dc.date.accessioned2018-03-28T23:21:06Z
dc.date.available2018-03-28T23:21:06Z
dc.identifierJournal Of Pediatric Endocrinology & Metabolism. Freund Publishing House Ltd, v. 11, n. 3, n. 465, n. 466, 1998.
dc.identifier0334-018X
dc.identifierWOS:000074603600011
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/61306
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/61306
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/61306
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1272150
dc.descriptionWe describe the identification of a single base mutation in the 5 alpha-reductase type II gene in a Brazilian patient who was reared as female and remained with female behavior and sexual identity.
dc.descriptiono TEXTO COMPLETO DESTE ARTIGO, ESTARÁ DISPONÍVEL À PARTIR DE AGOSTO DE 2015.
dc.description11
dc.description3
dc.description465
dc.description466
dc.languageen
dc.publisherFreund Publishing House Ltd
dc.publisherLondon
dc.publisherInglaterra
dc.relationJournal Of Pediatric Endocrinology & Metabolism
dc.relationJ. Pediatr. Endocrinol. Metab.
dc.rightsembargo
dc.sourceWeb of Science
dc.subjectmale pseudohermaphroditism
dc.subject5 alpha-reductase type II gene
dc.subjectpoint mutation
dc.subjectDeficiency
dc.titleDetection of Gly-196-Ser mutation in 5 alpha-reductase type II gene in a Brazilian patient with female assignment and behavior
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución