B-thalassemia intermedia and ivs - 1 nt6 homozygosis in brazil (1991)
- Autores:
- Autores USP: ZAGO, MARCO ANTONIO - FMRP ; COSTA, FERNANDO FERREIRA - FMRP
- Unidade: FMRP
- Assunto: MEDICINA INTERNA
- Idioma: Inglês
- Fonte:
- Título do periódico: 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: 23 abr. 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 abr. 23 ] -
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 abr. 23 ] - Analise de dna amplificado pela pcr na anemia falciforme e beta thalassemia
- 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
- Discrepancy between pit counting and spleen function tests in nutricional anemias and hemoglobinopathy C
- B+-thalassemia intermedia resulting from the interaction of the high hba2 and the silent b-thalassemia genes
- Asplenia e infeccao
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