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dc.contributor.CRUESPUniversidade Estadual de Campinaspt_BR
dc.typeArtigo de periódicopt_BR
dc.titleHemoglobin H disease resulting from the association of the - alpha(3.7) rightward deletion and the (alpha alpha)(MM) deletion in a Brazilian patientpt_BR
dc.contributor.authorWenning, MRSCpt_BR
dc.contributor.authorHarteveld, CLpt_BR
dc.contributor.authorGiordano, PCpt_BR
dc.contributor.authorKimura, EMpt_BR
dc.contributor.authorSaad, STOpt_BR
dc.contributor.authorCosta, FFpt_BR
dc.contributor.authorSonati, MFpt_BR
unicamp.authorState Univ Campinas UNICAMP, Sch Med Sci, Dept Clin Pathol, BR-13083970 Campinas, SP, Brazil State Univ Campinas UNICAMP, Sch Med Sci, Dept Clin Med, BR-13083970 Campinas, SP, Brazil Leiden Univ, Med Ctr, Dept Human & Clin Genet, Hemoglobinopathies Lab, Leiden, Netherlandspt_BR
dc.subjecthemoglobin H diseasept_BR
dc.subjectalpha-thalassemiapt_BR
dc.subjectalpha-globin genespt_BR
dc.subjectalpha-major regulatory elementpt_BR
dc.subjectSouth-American populationpt_BR
dc.subject.wosGlobin Genept_BR
dc.subject.wosThalassemiapt_BR
dc.subject.wosMutationspt_BR
dc.subject.wosLocuspt_BR
dc.description.abstractA patient with Hb H disease resulting from the association of the -alpha(3.7) rightward deletion with the rare (alphaalpha)(MM) deletion, which removes the entire alpha-major regulatory element (MRE), is reported. This is the first description of an alpha-thalassemic mutation resulting from deletion of the locus-controlling sequences in the South-American population.pt
dc.relation.ispartofEuropean Journal Of Haematologypt_BR
dc.relation.ispartofabbreviationEur. J. Haematol.pt_BR
dc.publisher.cityCopenhagenpt_BR
dc.publisher.countryDinamarcapt_BR
dc.publisherBlackwell Munksgaardpt_BR
dc.date.issued2002pt_BR
dc.date.monthofcirculationSEPpt_BR
dc.identifier.citationEuropean Journal Of Haematology. Blackwell Munksgaard, v. 69, n. 3, n. 179, n. 181, 2002.pt_BR
dc.language.isoenpt_BR
dc.description.volume69pt_BR
dc.description.issuenumber3pt_BR
dc.description.firstpage179pt_BR
dc.description.lastpage181pt_BR
dc.rightsfechadopt_BR
dc.sourceWeb of Sciencept_BR
dc.identifier.issn0902-4441pt_BR
dc.identifier.wosidWOS:000178849000008pt_BR
dc.identifier.doi10.1034/j.1600-0609.2002.02743.xpt_BR
dc.date.available2014-11-18T21:09:22Z
dc.date.available2015-11-26T17:54:22Z-
dc.date.accessioned2014-11-18T21:09:22Z
dc.date.accessioned2015-11-26T17:54:22Z-
dc.description.provenanceMade available in DSpace on 2014-11-18T21:09:22Z (GMT). No. of bitstreams: 1 WOS000178849000008.pdf: 151477 bytes, checksum: df0d2e291eefc9098da7f71113dfbaa3 (MD5) Previous issue date: 2002en
dc.description.provenanceMade available in DSpace on 2015-11-26T17:54:22Z (GMT). No. of bitstreams: 2 WOS000178849000008.pdf: 151477 bytes, checksum: df0d2e291eefc9098da7f71113dfbaa3 (MD5) WOS000178849000008.pdf.txt: 9578 bytes, checksum: d5c7a0e77c881c8afe2fccd71a1fe57b (MD5) Previous issue date: 2002en
dc.identifier.urihttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/68240pt_BR
dc.identifier.urihttp://www.repositorio.unicamp.br/handle/REPOSIP/68240
dc.identifier.urihttp://repositorio.unicamp.br/jspui/handle/REPOSIP/68240-
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