Hbf heterogeity in sickle cell anemia ando sickle cell beta-thalas-semia from brazil (1989)
- Authors:
- USP affiliated authors: TAVELLA, MARLI HAYDEE - FMRP ; ZAGO, MARCO ANTONIO - FMRP ; COSTA, FERNANDO FERREIRA - FMRP
- Unidade: FMRP
- Assunto: MEDICINA
- Language: Inglês
- Imprenta:
- Source:
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ABNT
ZAGO, M A e COSTA, F F e TAVELLA, M H. Hbf heterogeity in sickle cell anemia ando sickle cell beta-thalas-semia from brazil. Current Trends in Infant Screening. Tradução . Amsterdam: Elsevier, 1989. . . Acesso em: 13 fev. 2026. -
APA
Zago, M. A., Costa, F. F., & Tavella, M. H. (1989). Hbf heterogeity in sickle cell anemia ando sickle cell beta-thalas-semia from brazil. In Current Trends in Infant Screening. Amsterdam: Elsevier. -
NLM
Zago MA, Costa FF, Tavella MH. Hbf heterogeity in sickle cell anemia ando sickle cell beta-thalas-semia from brazil. In: Current Trends in Infant Screening. Amsterdam: Elsevier; 1989. [citado 2026 fev. 13 ] -
Vancouver
Zago MA, Costa FF, Tavella MH. Hbf heterogeity in sickle cell anemia ando sickle cell beta-thalas-semia from brazil. In: Current Trends in Infant Screening. Amsterdam: Elsevier; 1989. [citado 2026 fev. 13 ] - Alfa talassemia com deficiência gênica e anemia falciforme
- Heterogeneidade da hb f nas hemoglobinopatias
- Molecular bases beta thalassemia in brazil
- Associacao entre hb stanceyvite ii e talassemia com deficiencia genica de 3,7 hb
- Deletion type 'ALFA'-thalassemia among brazilian patients with sickle cell anemia
- Absence of the E2 allele of apolipoprotein in Amerindians
- Prevalence of FXIII VAL34LEU in the bratros (brazilian thrombosis study)
- B-thalassemia intermedia and ivs - 1 nt6 homozygosis in brazil
- Hereditary haemoglobin disorders in brazil
- Bone marrow and peripheral blood globin chain synthesis in sickle cell beta thalassaemia
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