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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/34398
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dc.contributor.authorBatista, DAS-
dc.contributor.authorViannamorgante, A. M.-
dc.contributor.authorZatz, M.-
dc.date.accessioned2014-05-20T15:23:38Z-
dc.date.accessioned2016-10-25T17:57:38Z-
dc.date.available2014-05-20T15:23:38Z-
dc.date.available2016-10-25T17:57:38Z-
dc.date.issued1990-12-01-
dc.identifierhttp://www.gmb.org.br/Revistas/V13/v13a79.pdf-
dc.identifier.citationRevista Brasileira de Genetica. Ribeirao Pret: Soc Brasil Genetica, v. 13, n. 4, p. 849-853, 1990.-
dc.identifier.issn0100-8455-
dc.identifier.urihttp://hdl.handle.net/11449/34398-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/34398-
dc.description.abstractWe studied cytogenetically 48 male patients with Duchenne or Becker muscular dystrophy. All of them showed normal X chromosomes. Fragility of Xp21 was investigated in 1400 G-banded chromosomes of 28 patients and only one break was observed at this band (0.07%). This low frequency of breakage excludes Xp21 as a fragile site in these patients.en
dc.format.extent849-853-
dc.language.isoeng-
dc.publisherSoc Brasil Genetica-
dc.sourceWeb of Science-
dc.titleCHROMOSOME-STUDIES IN MALES AFFECTED BY DUCHENNE OR BECKER MUSCULAR-DYSTROPHYen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUNIV ESTADUAL PAULISTA JULIO MESQUITA FILHO,INST BIOCIENCIAS,DEPT GENET,RUBIAO JR,BR-18610 BOTUCATU,SP,BRAZIL-
dc.description.affiliationUnespUNIV ESTADUAL PAULISTA JULIO MESQUITA FILHO,INST BIOCIENCIAS,DEPT GENET,RUBIAO JR,BR-18610 BOTUCATU,SP,BRAZIL-
dc.identifier.wosWOS:A1990EW22500020-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileWOSA1990EW22500020.pdf-
dc.relation.ispartofRevista Brasileira de Genética-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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