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Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-β-thalassemia in Northeast Thailand

✍ Scribed by Lalana Nuntakarn; Supan Fucharoen; Goonnapa Fucharoen; Kanokwan Sanchaisuriya; Arunee Jetsrisuparb; Surapon Wiangnon

Book ID
116304624
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
315 KB
Volume
42
Category
Article
ISSN
1079-9796

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✍ G. Schiliro'; P. Samperi; R. Testa; R. B. Gupta; L.-H. Gu; T. H. J. Huisman 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 546 KB

The clinical, hematological, and molecular features of 81 patients with Hb S-p-thalassemia and relatives from 76 unrelated families are reported. We analyzed the p-thalassemia mutations and the ps haplotypes in all patients and detected 6 different p-thalassemia alleles: codon 39 (C-tT) (39 cases),