Evaluation of HPLC and molecular genetic confirmatory testing as a starting point of national screening program for β-thalassemia carriers in Egyptians
Shaimaa Abdel Malik Hassan Pessar;
Abstract
Beta-Thalassemia (-thal) represents a major health problem in Egypt. It has been estimated that 1000 children out of 1.5 million live births are born annually with thalassemia major (TM) (El-Hashemite et al., 1997). In multi-center studies, the carrier r
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| Title | Evaluation of HPLC and molecular genetic confirmatory testing as a starting point of national screening program for β-thalassemia carriers in Egyptians | Other Titles | تقييم استخدام الفصل الكروماتوجرافى السائل عالى الآداء والتحليل الوراثي الجزيئى كبداية لبرنامج قومى لتحرى حاملى أنيميا البحر المتوسط من النوع بيتا فى المصريين | Authors | Shaimaa Abdel Malik Hassan Pessar | Keywords | Evaluation of HPLC and molecular genetic confirmatory testing as a starting point of national screening program for β-thalassemia carriers in Egyptians | Issue Date | 2011 | Description | Beta-Thalassemia (-thal) represents a major health problem in Egypt. It has been estimated that 1000 children out of 1.5 million live births are born annually with thalassemia major (TM) (El-Hashemite et al., 1997). In multi-center studies, the carrier r |
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