Esr detection of membrane alteration in hemoglobinopathies (1986)
- Authors:
- USP affiliated authors: ZAGO, MARCO ANTONIO - FMRP ; TABAK, MARCEL - IQSC ; BAFFA FILHO, OSWALDO - FFCLRP ; COSTA, FERNANDO FERREIRA - FMRP
- Unidades: FMRP; IQSC; FFCLRP
- Assunto: QUÍMICA
- Language: Inglês
- Source:
- Título: Bulletin of Magnetic Research
- Volume/Número/Paginação/Ano: v. 8 , n. 3-4, p. 190, 1986
-
ABNT
BAFFA, Oswaldo et al. Esr detection of membrane alteration in hemoglobinopathies. Bulletin of Magnetic Research, v. 8 , n. 3-4, p. 190, 1986Tradução . . Acesso em: 04 nov. 2024. -
APA
Baffa, O., Costa, F. F., Zago, M. A., & Tabak, M. (1986). Esr detection of membrane alteration in hemoglobinopathies. Bulletin of Magnetic Research, 8 ( 3-4), 190. -
NLM
Baffa O, Costa FF, Zago MA, Tabak M. Esr detection of membrane alteration in hemoglobinopathies. Bulletin of Magnetic Research. 1986 ; 8 ( 3-4): 190.[citado 2024 nov. 04 ] -
Vancouver
Baffa O, Costa FF, Zago MA, Tabak M. Esr detection of membrane alteration in hemoglobinopathies. Bulletin of Magnetic Research. 1986 ; 8 ( 3-4): 190.[citado 2024 nov. 04 ] - Hemichrome formation during hemoglobin zurich denaturation
- 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
- Hemicromos no patogenese de instabilidade da hb zurich
- 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
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