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Compound heterozygote state for GγAγ(δβ)°-thalassemia and hereditary persistence of fetal hemoglobin

✍ Scribed by Supan Fucharoen; Sitthichai Panyasai; Satja Surapot; Goonnapa Fucharoen; Kanokwan Sanchaisuriya

Publisher: John Wiley and Sons
Year: 2005
Tongue: English
Weight: 99 KB
Volume: 80
Category: Article
ISSN: 0361-8609
DOI: 10.1002/ajh.20426

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We studied a family in which two inherited defects of the non-␣-globin cluster segregate: Greek hereditary persistence of fetal hemoglobin (HPFH) and ␤-thalassemia. The compound heterozygote is a healthy man with 43% HbF, G ␥/ A ␥ ratio (27:73) differing from that of 10 simple heterozygotes for the