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β-Globin gene cluster haplotypes and HbF levels are not the only modulators of sickle cell disease in Lebanon

✍ Scribed by A. Inati; A. Taher; W. Bou Alawi W; S. Koussa; H. Kaspar; H. Shbaklo; P. A. Zalloua


Book ID
114423184
Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
121 KB
Volume
70
Category
Article
ISSN
0902-4441

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Effect of α-thalassemia and β-globin gen
✍ Figueiredo, M.S.; Kerbauy, J.; Gonçalves, M.S.; Arruda, V.R.; Saad, S.T.O.; Sona 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 447 KB 👁 1 views

To compare the features of sickle-cell anemia in Brazil with those in other locales, we studied the effects of the p-globin-like gene cluster haplotype and a-thalassemia upon the clinical and hematological features in 85 patients. The distribution of haplotypes differed from that in the United State