Unbalanced globin systhesis in bone marrow of beta-thalassemia heterozygotes (1988)
- Autores:
- Autores USP: ZAGO, MARCO ANTONIO - FMRP ; COSTA, FERNANDO FERREIRA - FMRP
- Unidade: FMRP
- Assunto: MEDICINA
- Idioma: Português
- Fonte:
- Título do periódico: Birth Defects: Original Article Series
- Volume/Número/Paginação/Ano: v.23, p.157-61, 1988
-
ABNT
COSTA, F F e ZAGO, M A e BOTTURA, C. Unbalanced globin systhesis in bone marrow of beta-thalassemia heterozygotes. Birth Defects: Original Article Series, v. 23, p. 157-61, 1988Tradução . . Acesso em: 19 abr. 2024. -
APA
Costa, F. F., Zago, M. A., & Bottura, C. (1988). Unbalanced globin systhesis in bone marrow of beta-thalassemia heterozygotes. Birth Defects: Original Article Series, 23, 157-61. -
NLM
Costa FF, Zago MA, Bottura C. Unbalanced globin systhesis in bone marrow of beta-thalassemia heterozygotes. Birth Defects: Original Article Series. 1988 ;23 157-61.[citado 2024 abr. 19 ] -
Vancouver
Costa FF, Zago MA, Bottura C. Unbalanced globin systhesis in bone marrow of beta-thalassemia heterozygotes. Birth Defects: Original Article Series. 1988 ;23 157-61.[citado 2024 abr. 19 ] - 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
- Analise de dna amplificado pela pcr na anemia falciforme e beta thalassemia
- 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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