Hemoglobin stanleyville ii (alpha 78 asn-lys) s associated with a 37-kb alpha-globin (1991)
- Authors:
- USP affiliated authors: ZAGO, MARCO ANTONIO - FMRP ; COSTA, FERNANDO FERREIRA - FMRP
- Unidade: FMRP
- Assunto: GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Human Genetics
- Volume/Número/Paginação/Ano: v.86, p.319-20, 1991
-
ABNT
COSTA, F F e SONATI, M F e ZAGO, M A. Hemoglobin stanleyville ii (alpha 78 asn-lys) s associated with a 37-kb alpha-globin. Human Genetics, v. 86, p. 319-20, 1991Tradução . . Acesso em: 23 abr. 2024. -
APA
Costa, F. F., Sonati, M. F., & Zago, M. A. (1991). Hemoglobin stanleyville ii (alpha 78 asn-lys) s associated with a 37-kb alpha-globin. Human Genetics, 86, 319-20. -
NLM
Costa FF, Sonati MF, Zago MA. Hemoglobin stanleyville ii (alpha 78 asn-lys) s associated with a 37-kb alpha-globin. Human Genetics. 1991 ;86 319-20.[citado 2024 abr. 23 ] -
Vancouver
Costa FF, Sonati MF, Zago MA. Hemoglobin stanleyville ii (alpha 78 asn-lys) s associated with a 37-kb alpha-globin. Human Genetics. 1991 ;86 319-20.[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
- 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
- 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
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
