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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/37011
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dc.contributor.authorBonini-Domingos, C. R.-
dc.contributor.authorZamaro, P. J.-
dc.contributor.authorMendiburu, C. F.-
dc.date.accessioned2014-05-20T15:26:57Z-
dc.date.accessioned2016-10-25T18:01:38Z-
dc.date.available2014-05-20T15:26:57Z-
dc.date.available2016-10-25T18:01:38Z-
dc.date.issued2003-06-01-
dc.identifier.citationClinical Chemistry. Washington: Amer Associação Clinical Chemistry, v. 49, n. 6, p. A7-A7, 2003.-
dc.identifier.issn0009-9147-
dc.identifier.urihttp://hdl.handle.net/11449/37011-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/37011-
dc.format.extentA7-A7-
dc.language.isoeng-
dc.publisherAmer Assoc Clinical Chemistry-
dc.sourceWeb of Science-
dc.titleFrequency of hereditary hemochromatosis gene mutations (C282Y and H63D) in hemoglobin S carrier from Brazil.en
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUNESP, Sao Jose do Rio Preto, SP, Brazil-
dc.description.affiliationUnespUNESP, Sao Jose do Rio Preto, SP, Brazil-
dc.identifier.wosWOS:000183088700018-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofClinical Chemistry-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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