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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/36521
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dc.contributor.authorScalco, F. B.-
dc.contributor.authorCorrea-Cerro, L. S.-
dc.contributor.authorWassif, C. A.-
dc.contributor.authorPorter, F. D.-
dc.contributor.authorMoretti-Ferreira, D.-
dc.date.accessioned2014-05-20T15:26:20Z-
dc.date.accessioned2016-10-25T18:00:56Z-
dc.date.available2014-05-20T15:26:20Z-
dc.date.available2016-10-25T18:00:56Z-
dc.date.issued2005-07-30-
dc.identifierhttp://dx.doi.org/10.1002/ajmg.a.30810-
dc.identifier.citationAmerican Journal of Medical Genetics Part A. Hoboken: Wiley-liss, v. 136A, n. 3, p. 278-281, 2005.-
dc.identifier.issn1552-4825-
dc.identifier.urihttp://hdl.handle.net/11449/36521-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/36521-
dc.format.extent278-281-
dc.language.isoeng-
dc.publisherWiley-Blackwell-
dc.sourceWeb of Science-
dc.titleDHCR7 mutations in Brazilian Smith-Lemli-Opitz syndrome patientsen
dc.typeoutro-
dc.contributor.institutionNICHHD-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationNICHHD, Heritable Disorders Branch, DHHS, Unit Mol Dysmorphol,NIH, Bethesda, MD 20892 USA-
dc.description.affiliationSão Paulo State Univ, Inst Biosci, Genet Counseling Serv, São Paulo, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Inst Biosci, Genet Counseling Serv, São Paulo, Brazil-
dc.identifier.doi10.1002/ajmg.a.30810-
dc.identifier.wosWOS:000230288400010-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofAmerican Journal of Medical Genetics Part A-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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