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DHCR7 mutations in Brazilian Smith-Lemli-Opitz syndrome patients

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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.contributor.institutionNICHHD
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:26:20Z
dc.date.available2014-05-20T15:26:20Z
dc.date.issued2005-07-30
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.format.extent278-281
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.doi10.1002/ajmg.a.30810
dc.identifier.issn1552-4825
dc.identifier.urihttp://hdl.handle.net/11449/36521
dc.identifier.wosWOS:000230288400010
dc.language.isoeng
dc.publisherWiley-Blackwell
dc.relation.ispartofAmerican Journal of Medical Genetics Part A
dc.relation.ispartofjcr2.264
dc.relation.ispartofsjr1,098
dc.rights.accessRightsAcesso abertopt
dc.sourceWeb of Science
dc.titleDHCR7 mutations in Brazilian Smith-Lemli-Opitz syndrome patientsen
dc.typeCartapt
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dcterms.rightsHolderWiley-Blackwell
dspace.entity.typePublication
relation.isOrgUnitOfPublicationab63624f-c491-4ac7-bd2c-767f17ac838d
relation.isOrgUnitOfPublication.latestForDiscoveryab63624f-c491-4ac7-bd2c-767f17ac838d
unesp.author.orcid0000-0002-2524-1420[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.departmentGenética - IBBpt

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