B-thalassemia intermedia and ivs - 1 nt6 homozygosis in brazil (1991)
- Authors:
- USP affiliated authors: ZAGO, MARCO ANTONIO - FMRP ; COSTA, FERNANDO FERREIRA - FMRP
- Unidade: FMRP
- Assunto: MEDICINA INTERNA
- Language: Inglês
- Source:
- Título: Brazilian Journal of Medical and Biological Research
- Volume/Número/Paginação/Ano: v.24, p.157-61, 1991
-
ABNT
COSTA, F F e TAVELLA, M H e ZAGO, M A. B-thalassemia intermedia and ivs - 1 nt6 homozygosis in brazil. Brazilian Journal of Medical and Biological Research, v. 24, p. 157-61, 1991Tradução . . Acesso em: 04 out. 2024. -
APA
Costa, F. F., Tavella, M. H., & Zago, M. A. (1991). B-thalassemia intermedia and ivs - 1 nt6 homozygosis in brazil. Brazilian Journal of Medical and Biological Research, 24, 157-61. -
NLM
Costa FF, Tavella MH, Zago MA. B-thalassemia intermedia and ivs - 1 nt6 homozygosis in brazil. Brazilian Journal of Medical and Biological Research. 1991 ;24 157-61.[citado 2024 out. 04 ] -
Vancouver
Costa FF, Tavella MH, Zago MA. B-thalassemia intermedia and ivs - 1 nt6 homozygosis in brazil. Brazilian Journal of Medical and Biological Research. 1991 ;24 157-61.[citado 2024 out. 04 ] - 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
- Hb d-los angeles in brazil: simple heterozygotes and associations with beta-thalassemia and with hb s
- Brazilian type of nondeletional a gamma hereditary persistence of fetal hemoglobin has ac-q substitution
- Hereditary haemoglobin disorders in brazil
- Bone marrow and peripheral blood globin chain synthesis in sickle cell beta thalassaemia
- Analise de dna amplificado pela pcr na anemia falciforme e beta thalassemia
- Hemichrome formation during hemoglobin zurich denaturation
- Hbf heterogeity in sickle cell anemia ando sickle cell beta-thalas-semia from brazil
- Homoglobinopatias no estado de sao paulo
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas