Evaluation of Red Blood Cell Alloantibodies in Thalassemic Patients
Salah Shehata Abu El-Yazed;
Abstract
The thalassemias are hereditary hemolytic anemias characterized by reduced or absent synthesis of one or more of the globin chains of hemoglobin leading to globin chain imbalance
The most important forms of thalassemia result from autosomal mutant genes t
The most important forms of thalassemia result from autosomal mutant genes t
Other data
| Title | Evaluation of Red Blood Cell Alloantibodies in Thalassemic Patients | Authors | Salah Shehata Abu El-Yazed | Keywords | Evaluation of Red Blood Cell Alloantibodies in Thalassemic Patients | Issue Date | 2006 | Description | The thalassemias are hereditary hemolytic anemias characterized by reduced or absent synthesis of one or more of the globin chains of hemoglobin leading to globin chain imbalance The most important forms of thalassemia result from autosomal mutant genes t |
Recommend this item
Similar Items from Core Recommender Database
Items in Ain Shams Scholar are protected by copyright, with all rights reserved, unless otherwise indicated.