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: 29 dez. 2025. -
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 2025 dez. 29 ] -
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 2025 dez. 29 ] - 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
- Alfa talassemia com deficiência gênica e anemia falciforme
- Deletion type 'ALFA'-thalassemia among brazilian patients with sickle cell anemia
- Unbalanced globin systhesis in bone marrow of beta-thalassemia heterozygotes
- Hemoglobin stanleyville ii (alpha 78 asn-lys) s associated with a 37-kb alpha-globin
- B-thalassemia intermedia and ivs - 1 nt6 homozygosis in brazil
- Prevalence of FXIII VAL34LEU in the bratros (brazilian thrombosis study)
- Absence of the E2 allele of apolipoprotein in Amerindians
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