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CHROMOSOME-STUDIES IN MALES AFFECTED BY DUCHENNE OR BECKER MUSCULAR-DYSTROPHY

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dc.contributor.authorBatista, DAS
dc.contributor.authorViannamorgante, A. M.
dc.contributor.authorZatz, M.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:23:38Z
dc.date.available2014-05-20T15:23:38Z
dc.date.issued1990-12-01
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.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.format.extent849-853
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.fileWOSA1990EW22500020.pdf
dc.identifier.issn0100-8455
dc.identifier.urihttp://hdl.handle.net/11449/34398
dc.identifier.wosWOS:A1990EW22500020
dc.language.isoeng
dc.publisherSoc Brasil Genetica
dc.relation.ispartofRevista Brasileira de Genética
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.titleCHROMOSOME-STUDIES IN MALES AFFECTED BY DUCHENNE OR BECKER MUSCULAR-DYSTROPHYen
dc.typeArtigo
dcterms.licensehttp://www.scielo.br/revistas/bjg/paboutj.htm
dcterms.rightsHolderSoc Brasil Genetica
dspace.entity.typePublication
unesp.author.orcid0000-0003-3970-8025[3]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências, Botucatupt
unesp.departmentGenética - IBBpt

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Botucatu - IBB - Instituto de Biociências