Hb d-los angeles in brazil: simple heterozygotes and associations with beta-thalassemia and with hb s (1988)
- Authors:
- USP affiliated authors: ZAGO, MARCO ANTONIO - FMRP ; COSTA, FERNANDO FERREIRA - FMRP
- Unidade: FMRP
- Assunto: HEMATOLOGIA
- Language: Português
- Source:
- Título: Hemoglobin
- Volume/Número/Paginação/Ano: v.12, n.4 , p.399-403, 1988
-
ABNT
ZAGO, M A e COSTA, F F. Hb d-los angeles in brazil: simple heterozygotes and associations with beta-thalassemia and with hb s. Hemoglobin, v. 12, n. 4 , p. 399-403, 1988Tradução . . Acesso em: 29 dez. 2025. -
APA
Zago, M. A., & Costa, F. F. (1988). Hb d-los angeles in brazil: simple heterozygotes and associations with beta-thalassemia and with hb s. Hemoglobin, 12( 4 ), 399-403. -
NLM
Zago MA, Costa FF. Hb d-los angeles in brazil: simple heterozygotes and associations with beta-thalassemia and with hb s. Hemoglobin. 1988 ;12( 4 ): 399-403.[citado 2025 dez. 29 ] -
Vancouver
Zago MA, Costa FF. Hb d-los angeles in brazil: simple heterozygotes and associations with beta-thalassemia and with hb s. Hemoglobin. 1988 ;12( 4 ): 399-403.[citado 2025 dez. 29 ] - 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
- 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
- Homoglobinopatias no estado de sao paulo
- Interacao de alfatalassemia e hemoglobina stanleyville ii (alfa 78-> lis)
- Hemichrome formation during hemoglobin zurich denaturation
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