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Sickle cell–haemoglobin E (HbSE) compound heterozygosity: a clinical and haematological study

✍ Scribed by H. H. M. KNOX-MACAULAY; M. M. AHMED; D. GRAVELL; S. AL-KINDI; A. GANESH


Book ID
108702837
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
602 KB
Volume
29
Category
Article
ISSN
1751-5521

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✍ Bienzle, U. ;Kappes, R. ;Reimer, A. ;Feldheim, M. ;Tischendorf, F. W. ;Kohne, E. 📂 Article 📅 1983 🏛 Springer-Verlag ⚖ 354 KB

Clinical and haematological features of 20 patients of several Liberian ethnic groups with sickle cell-beta +-thalassaemia are reported. Haemoglobin analysis showed increased Hb A2 values, high Hb A levels (median 25%), variable amounts of Hb F and a slight imbalance of non alpha/alpha globin chain