Different Types of Complications in Patients Suffering from B-Thalassemia (Thalassemia Major)
INTRODUCTION Thalassemia is a heterogeneous group of gene disorders caused byan inherited mutation or deletion of genes at chromosome 16 & 11 resulting in decreased synthesis of adult hemoglobin. Its incidence is higher in people/children having a positive family history of Thalassemia Among its...
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| Format: | Book |
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Gandhara University,
2017-09-01T00:00:00Z.
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A1234.567 |
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