PREVALENCE OF Β-THALASSEMIA TRAIT IN DEFERRED ANAEMIC (VOLUNTARY, NON-REMUNERATED) BLOOD DONORS
Mohamed Sayd El-Badie Mohamed Abd Al-Hadi;
Abstract
T
halassemia is a heterogeneous group of congenital hemoglobinopathies caused by mutations in the globin gene complex that result in an imbalance in globin synthesis.
Screening for -thalassaemia is difficult, mainly because of heterogeneity of -thal
halassemia is a heterogeneous group of congenital hemoglobinopathies caused by mutations in the globin gene complex that result in an imbalance in globin synthesis.
Screening for -thalassaemia is difficult, mainly because of heterogeneity of -thal
Other data
| Title | PREVALENCE OF Β-THALASSEMIA TRAIT IN DEFERRED ANAEMIC (VOLUNTARY, NON-REMUNERATED) BLOOD DONORS | Other Titles | الكشف عن حاملي مرض أنيميا البحر المتوسط بين متبرعي الدم المتطوعين المستبعدين مؤقتا بسبب الأنيميا | Authors | Mohamed Sayd El-Badie Mohamed Abd Al-Hadi | Keywords | PREVALENCE OF Β-THALASSEMIA TRAIT IN DEFERRED ANAEMIC (VOLUNTARY, NON-REMUNERATED) BLOOD DONORS | Issue Date | 2011 | Description | T halassemia is a heterogeneous group of congenital hemoglobinopathies caused by mutations in the globin gene complex that result in an imbalance in globin synthesis. Screening for -thalassaemia is difficult, mainly because of heterogeneity of -thal |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 106832p4203.pdf | 845.3 kB | Adobe PDF | View/Open |
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