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Non-anemic homozygous βo thalassemia in an African-American family: Association of high fetal hemoglobin levels with β thalassemia alleles

✍ Scribed by Vladimir Divoky; Michal Mrug; Denyse Thornley-Brown; Martina Divoka; Josef T. Prchal

Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
176 KB
Volume
68
Category
Article
ISSN
0361-8609

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✍ Tadmouri, G. O.; Yüksel, L.; Başak, A. N. 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 36 KB

␤-thalassemia and sickle cell disease (SCD) are common disorders in Turkey. Compound heterozygosity for these two disorders (␤ S /␤-thalassemia) is encountered frequently. In this report we present hematological and molecular data of two Turkish siblings with ␤ S /␤ del -thalassemia caused by a 290