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

Detalhes bibliográficos
Autor(a) principal: Batista, DAS
Data de Publicação: 1990
Outros Autores: Viannamorgante, A. M., Zatz, M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://www.gmb.org.br/Revistas/V13/v13a79.pdf
http://hdl.handle.net/11449/34398
Resumo: We 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.
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spelling CHROMOSOME-STUDIES IN MALES AFFECTED BY DUCHENNE OR BECKER MUSCULAR-DYSTROPHYWe 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.UNIV ESTADUAL PAULISTA JULIO MESQUITA FILHO,INST BIOCIENCIAS,DEPT GENET,RUBIAO JR,BR-18610 BOTUCATU,SP,BRAZILUNIV ESTADUAL PAULISTA JULIO MESQUITA FILHO,INST BIOCIENCIAS,DEPT GENET,RUBIAO JR,BR-18610 BOTUCATU,SP,BRAZILSoc Brasil GeneticaUniversidade Estadual Paulista (Unesp)Batista, DASViannamorgante, A. M.Zatz, M.2014-05-20T15:23:38Z2014-05-20T15:23:38Z1990-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article849-853application/pdfhttp://www.gmb.org.br/Revistas/V13/v13a79.pdfRevista Brasileira de Genetica. Ribeirao Pret: Soc Brasil Genetica, v. 13, n. 4, p. 849-853, 1990.0100-8455http://hdl.handle.net/11449/34398WOS:A1990EW22500020WOSA1990EW22500020.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengRevista Brasileira de Genéticainfo:eu-repo/semantics/openAccess2023-10-14T06:08:13Zoai:repositorio.unesp.br:11449/34398Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-10-14T06:08:13Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv CHROMOSOME-STUDIES IN MALES AFFECTED BY DUCHENNE OR BECKER MUSCULAR-DYSTROPHY
title CHROMOSOME-STUDIES IN MALES AFFECTED BY DUCHENNE OR BECKER MUSCULAR-DYSTROPHY
spellingShingle CHROMOSOME-STUDIES IN MALES AFFECTED BY DUCHENNE OR BECKER MUSCULAR-DYSTROPHY
Batista, DAS
title_short CHROMOSOME-STUDIES IN MALES AFFECTED BY DUCHENNE OR BECKER MUSCULAR-DYSTROPHY
title_full CHROMOSOME-STUDIES IN MALES AFFECTED BY DUCHENNE OR BECKER MUSCULAR-DYSTROPHY
title_fullStr CHROMOSOME-STUDIES IN MALES AFFECTED BY DUCHENNE OR BECKER MUSCULAR-DYSTROPHY
title_full_unstemmed CHROMOSOME-STUDIES IN MALES AFFECTED BY DUCHENNE OR BECKER MUSCULAR-DYSTROPHY
title_sort CHROMOSOME-STUDIES IN MALES AFFECTED BY DUCHENNE OR BECKER MUSCULAR-DYSTROPHY
author Batista, DAS
author_facet Batista, DAS
Viannamorgante, A. M.
Zatz, M.
author_role author
author2 Viannamorgante, A. M.
Zatz, M.
author2_role author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Batista, DAS
Viannamorgante, A. M.
Zatz, M.
description We 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.
publishDate 1990
dc.date.none.fl_str_mv 1990-12-01
2014-05-20T15:23:38Z
2014-05-20T15:23:38Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://www.gmb.org.br/Revistas/V13/v13a79.pdf
Revista Brasileira de Genetica. Ribeirao Pret: Soc Brasil Genetica, v. 13, n. 4, p. 849-853, 1990.
0100-8455
http://hdl.handle.net/11449/34398
WOS:A1990EW22500020
WOSA1990EW22500020.pdf
url http://www.gmb.org.br/Revistas/V13/v13a79.pdf
http://hdl.handle.net/11449/34398
identifier_str_mv Revista Brasileira de Genetica. Ribeirao Pret: Soc Brasil Genetica, v. 13, n. 4, p. 849-853, 1990.
0100-8455
WOS:A1990EW22500020
WOSA1990EW22500020.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Revista Brasileira de Genética
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 849-853
application/pdf
dc.publisher.none.fl_str_mv Soc Brasil Genetica
publisher.none.fl_str_mv Soc Brasil Genetica
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1792961549161201664

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