Finlay-Marks (SEN) syndrome: A sporadic case and the delineation of the syndrome

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dc.contributor.author Sobreira, NLD
dc.contributor.author Brunoni, D.
dc.contributor.author Cernach, MCSP
dc.contributor.author Perez, ABA
dc.date.accessioned 2016-01-24T12:40:56Z
dc.date.available 2016-01-24T12:40:56Z
dc.date.issued 2006-02-01
dc.identifier http://dx.doi.org/10.1002/ajmg.a.31063
dc.identifier.citation American Journal of Medical Genetics Part A. Hoboken: Wiley-liss, v. 140A, n. 3, p. 300-302, 2006.
dc.identifier.issn 1552-4825
dc.identifier.uri http://repositorio.unifesp.br/handle/11600/28715
dc.format.extent 300-302
dc.language.iso eng
dc.publisher Wiley-Blackwell
dc.relation.ispartof American Journal of Medical Genetics Part A
dc.rights Acesso restrito
dc.title Finlay-Marks (SEN) syndrome: A sporadic case and the delineation of the syndrome en
dc.type Carta
dc.rights.license http://olabout.wiley.com/WileyCDA/Section/id-406071.html
dc.contributor.institution Universidade Federal de São Paulo (UNIFESP)
dc.description.affiliation UNIFESP, EPM, Ctr Genet Med, Dept Morfol & Pediat, BR-04020023 São Paulo, Brazil
dc.description.affiliationUnifesp UNIFESP, EPM, Ctr Genet Med, Dept Morfol & Pediat, BR-04020023 São Paulo, Brazil
dc.identifier.doi 10.1002/ajmg.a.31063
dc.description.source Web of Science
dc.identifier.wos WOS:000235264400019



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