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Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients

✍ Scribed by Jouini, L.; Sahli, C. A.; Laaouini, N.; Ouali, F.; Youssef, I. Ben; Dakhlaoui, B.; Othmeni, R.; Ouennich, F.; Fredj, S. Hadj; Siala, H.; Becher, M.; Toumi, N. E.; Fattoum, S.; Hafsia, R.; Bibi, A.; Messaoud, T.


Book ID
121427412
Publisher
Springer
Year
2013
Tongue
English
Weight
245 KB
Volume
40
Category
Article
ISSN
0301-4851

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Heterogeneity in β0thalassemia from Alge
✍ Mériem Belhani; F. Morlé; P. Colonna; Jacqueline Godet 📂 Article 📅 1980 🏛 Springer 🌐 English ⚖ 537 KB

Six Algerian patients with beta 0 thalassemia are presented, in addition to the two patients already reported (Godet et al., 1977). Family studies indicate that all the patients had homozygous beta thalassemia characterized by absence of beta globin chain synthesis in peripheral blood. The clinical