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

dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:23:38Z
dc.date.available2014-05-20T15:23:38Z
dc.date.created2014-05-20T15:23:38Z
dc.date.issued1990-12-01
dc.identifierRevista Brasileira de Genetica. Ribeirao Pret: Soc Brasil Genetica, v. 13, n. 4, p. 849-853, 1990.
dc.identifier0100-8455
dc.identifierhttp://hdl.handle.net/11449/34398
dc.identifierWOS:A1990EW22500020
dc.identifierWOSA1990EW22500020.pdf
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.
dc.languageeng
dc.publisherSoc Brasil Genetica
dc.relationRevista Brasileira de Genética
dc.rightsAcesso aberto
dc.sourceWeb of Science
dc.titleCHROMOSOME-STUDIES IN MALES AFFECTED BY DUCHENNE OR BECKER MUSCULAR-DYSTROPHY
dc.typeArtículos de revistas


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