REFERENCES
- Bunn HF, Forget BG. Sickle cell disease-molecular and cellular pathogenesis. Hemoglobin: Molecular, Genetic and Clinical Aspects, HF Bunn, BG Forget. Saunders Company, Philadelphia 1986; 453–501
- Ramalho AS, Teixeira RC, Teixeira PA. Genética e saúde pública noBrasil: os programas comunitários de hemoglobinopatias hereditárias. An Acad Nac Med 1996; 156(1)13–18
- Bandeira FMGC, Leal MC, Souza RR, Furtado VC, Gomes YM, Marques M. Características de recém-nascidos portadores de hemoglobinas S detectados através de triagem de sangue de cordão umbilical. J Pediatr 1999; 75(3)167–171
- Nagel RL, Steinberg MH. Genetics of the βS gene: origins, genetic epidemiology, and epistasis in sickle cell anemia. Disorders of Hemoglobin – Genetics, Pathophysiology, and Management, MH Steinberg, BG Forget, DR Higgs, RL Nagel. University Press, Cambridge 2001; 711–755
- Steinberg MH, Nagel RL, Lawrence C, Swaminathan V, Lu ZH, Plonczynski M, Harrell A. β-Globin gene haplotype in Hb SC disease. Am J Hematol 1996; 52(3)189–191
- Pagnier J, Mears G, Dunda-Belkhodja O, Schaefer-Rego KE, Beldjord C, Nagel RL, Labie D. Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa. Proc Natl Acad Sci USA 1984; 81(6)1771–1773
- Zago MA, Figueiredo MS, Ogo SH. Bantu βS cluster haplotype predominates among Brazilian Blacks. Am J Phys Anthropol 1992; 88(3)295–298
- Figueiredo MS, Kerbauy J, Gonçalves MS, Arruda VR, Saad STO, Sonat MF, Stoming T, Costa FF. Effect of α-thalassemia and β-globin gene cluster haplotypes on the hematological and clinical features of sickle cell anemia in Brazil. Am J Hematol 1996; 53(2)72–76
- Adorno EV, Zanette A, Lyra I, Souza CC, Santos LF, Menezes JF, Dupuit MF, Almeida MNT, Reis MG, Souza Gonçalves M. The β-globin gene cluster haplotypes in sickle cell anemia patients from Northeast Brazil: a clinical and molecular view. Hemoglobin 2004; 28(3)267–271
- Naoum PC. Eletroforese. Técnicas e diagnósticos. Livraria Editora Santos, São Paulo 1990
- Dodé C, Krishnamoorthy R, Lamb J, Rochete J. Rapid analysis of −α3.7 thalassaemia and αanti 3.7 by enzymatic amplification analysis. Br J Haematol 1992; 2(1)105–111
- Sutton M, Bouhassira EE, Nagel RL. Polymerase chain reaction amplification applied to the determination of β-like globin gene cluster haplotypes. Am J Hematol 1989; 32(1)66–69
- Galiza Neto GC, Pitombeira HHS, Magalhães SMM. Análise dos haplótipos do gene da βS em falcêmicos no Ceará – Brasil. Ann Braz J Hematol Hemother 2004; 26(S2)9, (abstract)
- Pante-De-Sousa G, Mousinho-Ribeiro RC, Santos EJM, Zago MA, Guerreiro JF. Origin of the Hemoglobin S gene in a northern Brazilian population: the combined effects of slave trade and internal migrations. Genet Mol Biol 1998; 21(4)1–9
- Wagner S, Friedrish J, Job F, Hutz M. Caracterização molecular de pacientes com anemia falciforme de Porto Alegre. Ann Genet Mol Biol 1996; 19(Suppl)244, (abstract)
- Curtain PD. The Atlantic Slave Trade: a Census. University of Wisconsin Press, Milwaukee 1969
- Sousa CC, Adorno EV, Zanette A, Lyra I, Gonçalves MS. Caracterização dos haplótipos e correlação com as principais manifestações clínicas em 45 indivíduos portadores da doença SC em Salvador, Bahia. Ann Braz Hematol Hemother 2003; 25(S2)16, (abstract)
- Antonarakis SE, Kazazian HH, Jr, Orkin SH. DNA polymorphism and molecular pathology of the human globin gene clusters. Hum Genet 1985; 69(1)1–14
- Kazazian HH, Jr, Orkin SH, Antonarakis SE, Sexton JP, Boehm CD, Goff SC, Waber PG. Molecular characterization of seven β-thalassemia mutations in Asian Indians. EMBO J 1984; 3(3)593–596
- Romana M, Keclard L, Guillemin G, Lavocat E, Saint-Martin C, Berchel C, Merault G. Molecular characterization of β-thalassemia mutations in Guadaloupe. Am J Hematol 1996; 53(4)228–233