Zobrazeno 1 - 4
of 4
pro vyhledávání: '"F A, Codrington"'
Autor:
J. H. Wisse, J. F. Codrington, Ferdane Kutlar, J. Anijs, Titus H.J. Huisman, H.-W. Li, F. A. Codrington, M. Ramachandran
Publikováno v:
Acta Haematologica. 84:135-138
Hematological and hemoglobin composition data are presented for 14 members of a Surinam family (and for 1 unrelated subject) with either a β-thalassemia heterozygosity [5 with the -29 (A – G) β+
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6a77d849e60145b146ec423ed275374
https://doi.org/10.1159/000205050
https://doi.org/10.1159/000205050
Autor:
J, Codrington, J, Anijs, J H, Wisse, F A, Codrington, H W, Li, F, Kutlar, M, Ramachandran, T H, Huisman
Publikováno v:
Acta haematologica. 84(3)
Hematological and hemoglobin composition data are presented for 14 members of a Surinam family (and for 1 unrelated subject) with either a beta-thalassemia heterozygosity [5 with the -29 (A----G) beta + mutation and 5 with the IVS II-849 (A----G) bet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d51d0339243f929d1753e0fc07cddd11
https://pubmed.ncbi.nlm.nih.gov/2123063
https://pubmed.ncbi.nlm.nih.gov/2123063
Autor:
J. H. Wisse, J. F. Codrington, S. C. Wong, J. B. Wilson, F. A. Codrington, Brooke B. Webber, Titus H.J. Huisman
Publikováno v:
Hemoglobin. 13:543-556
Three different hemoglobinopathies, i.e. Hb S, Hb Chad [alpha 23 (B4)Glu----Lys], and alpha-thalassemia-2 (-3.7) have been observed in eight members of a family from Surinam. The proposita had all three abnormalities, while her mother and four of her
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab08f9fdd8ec2f6d13d896349e256b0c
https://doi.org/10.3109/03630268908993105
https://doi.org/10.3109/03630268908993105
Autor:
B. M., Winifred Hulbert, F. I. Codrington, Jean Moore Cavell, Edith Eberle, Grace McGavran, Frank C. Laubach
Publikováno v:
Pacific Affairs. 3:312
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f83fe6c9e2d0a406316d457de9448ca6
https://doi.org/10.2307/2749878
https://doi.org/10.2307/2749878