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Study of genetic heterogeneity of hemoglobinopathy and β-thalassemia molecular variants in newborns

✍ Scribed by R. F. Mamedova


Book ID
111498315
Publisher
Allerton Press, Inc.
Year
2011
Tongue
English
Weight
644 KB
Volume
26
Category
Article
ISSN
0891-4168

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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