HBH DISEASE ASSOCIATED WITH THE (--MED) DELETION IN A BRAZILIAN BLACK WOMAN

dc.creatorSONATI, MF
dc.creatorKIMURA, EM
dc.creatorGROTTO, HZW
dc.creatorTAVELLA, MH
dc.creatorCOSTA, FF
dc.date1992
dc.date2014-07-30T17:52:47Z
dc.date2015-11-26T16:44:20Z
dc.date2014-07-30T17:52:47Z
dc.date2015-11-26T16:44:20Z
dc.date.accessioned2018-03-28T23:29:38Z
dc.date.available2018-03-28T23:29:38Z
dc.identifierActa Haematologica. Karger, v. 87, n. 3, n. 145, n. 147, 1992.
dc.identifier0001-5792
dc.identifierWOS:A1992JF30300007
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/68617
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/68617
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1273885
dc.descriptionClinical, laboratory features and restriction enzyme DNA analysis are reported for a black Brazilian woman with HbH disease. The patient presented a thalassemic blood picture with HbH and Hb Bart's. Gene mapping demonstrated the compound heterozygous state for the --MED and -alpha-3.7 deletions.
dc.description87
dc.description3
dc.description145
dc.description147
dc.languageen
dc.publisherKarger
dc.publisherBasel
dc.publisherSuíça
dc.relationActa Haematologica
dc.relationActa Haematol.
dc.rightsfechado
dc.rightshttp://www.karger.com/Services/RightsPermissions
dc.sourceWeb of Science
dc.subjectALPHA-GENE DELETION
dc.subjectHBH DISEASE
dc.subjectALPHA-THALASSEMIA
dc.subjectAlpha-thalassemia Haplotypes
dc.subjectHemoglobin-h Disease
dc.subjectGene Deletions
dc.subjectPopulation
dc.subjectGlobin
dc.titleHBH DISEASE ASSOCIATED WITH THE (--MED) DELETION IN A BRAZILIAN BLACK WOMAN
dc.typeArtículos de revistas


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