Zobrazeno 1 - 3
of 3
pro vyhledávání: '"C. T. A. Acquaye"'
Autor:
Walter A. Schroeder, C. T. A. Acquaye, F.I.D. Konotey-Ahulu, B. Ringelhann, Titus H.J. Huisman, P. K. Sukumaran, G. Yawson, J. H. Oldham
Publikováno v:
Biochemical Genetics. 15:1083-1096
Two sons of a previously reported Ghanaian homozygote for the hereditary persistence of fetal hemoglobin (HPFH) (Ringelhann et al., 1970) also are HPFH homozygotes. In addition, another unrelated adult Ghanaian homozygote has been detected. All of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7264f19735dd2b309111d0b06af1e741
https://doi.org/10.1007/bf00484499
https://doi.org/10.1007/bf00484499
Autor:
C. T. A. Acquaye, Barbara Giglioni, Elio Polli, Giuseppe Masera, Sergio Ottolenghi, A. M. Gianni, Paola Comi, J. H. Oldham
Publikováno v:
Nature. 278:654-657
THE thalassaemias are a group of inherited disorders characterised by the defective production of either α (α thalassaemias) or non-α (β and δ°β° thalassaemias) globin chains of haemoglobins (Hb)1. In β thalassaemias the decreased synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52cbedadee455ac97433dd64df794bcc
https://doi.org/10.1038/278654a0
https://doi.org/10.1038/278654a0
Publikováno v:
The Lancet. 309:796-797
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c542502c1d53f96bfe26a2ea49436fc
https://doi.org/10.1016/s0140-6736(77)92977-4
https://doi.org/10.1016/s0140-6736(77)92977-4