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Search on : SONATI, MARIA DE FATIMA [Author]
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 Pereira, Julio Abayuba da Luz et al. Hb Southampton [B106(G8)LeuPRO, CTGCCG] in a Uruguayan woman. Rev. Bras. Hematol. Hemoter., 2013, vol.35, no.2, p.146-147. ISSN 1516-8484
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 Sonati, Maria de Fátima. α-chain hemoglobin variants with electrophoretic mobility similar to that of hemoglobin S in newborn screening programs. Rev. Bras. Hematol. Hemoter., 2013, vol.35, no.2, p.85-86. ISSN 1516-8484
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 Kimura, Elza M. et al. Identificação e caracterização de variantes novas e raras da hemoglobina humana. Rev. Bras. Hematol. Hemoter., Ago 2008, vol.30, no.4, p.316-319. ISSN 1516-8484


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 Sonati, Maria de Fátima and Costa, Fernando Ferreira Genética das doenças hematológicas: as hemoglobinopatias hereditárias. J. Pediatr. (Rio J.), Ago 2008, vol.84, no.4, p.S40-S51. ISSN 0021-7557


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 Campregher, Paulo Vidal et al. Haptoglobin phenotypes in Brazilian patients with leukemia. J. Bras. Patol. Med. Lab., Oct 2004, vol.40, no.5, p.307-309. ISSN 1676-2444


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 Luz, Julio Da et al. Frequency and spectrum of hemoglobinopathy mutations in a Uruguayan pediatric population. Genet. Mol. Biol., 2013, vol.36, no.3, p.316-322. ISSN 1415-4757
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 Alcoforado, Gustavo Henrique de Medeiros et al. Prevalence of α-thalassemia 3.7 kb deletion in the adult population of Rio Grande do Norte, Brazil. Genet. Mol. Biol., 2012, vol.35, no.3, p.594-598. ISSN 1415-4757
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 Silveira, Zama Messala Luna da et al. Characterization of beta-thalassemia mutations in patients from the state of Rio Grande do Norte, Brazil. Genet. Mol. Biol., 2011, vol.34, no.3, p.425-428. ISSN 1415-4757
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 Cabral, Cynthia Hatsue Kitayama et al. Determination of βS haplotypes in patients with sickle-cell anemia in the state of Rio Grande do Norte, Brazil. Genet. Mol. Biol., 2011, vol.34, no.3, p.421-424. ISSN 1415-4757
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 Kimura, Elza M. et al. Hb H disease resulting from the association of an αº-thalassemia allele [-(α)20.5] with an unstable α-globin variant [Hb Icaria]: first report on the occurrence in Brazil. Genet. Mol. Biol., 2009, vol.32, no.4, p.712-715. ISSN 1415-4757
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