Hereditary haemoglobin disorders in brazil (1985)
- Authors:
- USP affiliated authors: ZAGO, MARCO ANTONIO - FMRP ; COSTA, FERNANDO FERREIRA - FMRP
- Unidade: FMRP
- DOI: 10.1016/0035-9203(85)90389-x
- Assunto: ANEMIA FALCIFORME
- Language: Português
- Source:
- Título: Transactions of the Royal Society of Tropical Medicine and Hygiene
- Volume/Número/Paginação/Ano: v.79, p.385, 1985
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
ZAGO, M A e COSTA, F F. Hereditary haemoglobin disorders in brazil. Transactions of the Royal Society of Tropical Medicine and Hygiene, v. 79, p. 385, 1985Tradução . . Disponível em: https://doi.org/10.1016/0035-9203(85)90389-x. Acesso em: 29 dez. 2025. -
APA
Zago, M. A., & Costa, F. F. (1985). Hereditary haemoglobin disorders in brazil. Transactions of the Royal Society of Tropical Medicine and Hygiene, 79, 385. doi:10.1016/0035-9203(85)90389-x -
NLM
Zago MA, Costa FF. Hereditary haemoglobin disorders in brazil [Internet]. Transactions of the Royal Society of Tropical Medicine and Hygiene. 1985 ;79 385.[citado 2025 dez. 29 ] Available from: https://doi.org/10.1016/0035-9203(85)90389-x -
Vancouver
Zago MA, Costa FF. Hereditary haemoglobin disorders in brazil [Internet]. Transactions of the Royal Society of Tropical Medicine and Hygiene. 1985 ;79 385.[citado 2025 dez. 29 ] Available from: https://doi.org/10.1016/0035-9203(85)90389-x - 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
- 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
- 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
- Homoglobinopatias no estado de sao paulo
- Interacao de alfatalassemia e hemoglobina stanleyville ii (alfa 78-> lis)
- Hemichrome formation during hemoglobin zurich denaturation
Informações sobre o DOI: 10.1016/0035-9203(85)90389-x (Fonte: oaDOI API)
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