Omnia Yahia Ibrahim Abdeldayem <br/><br/>
G6PD gene polymorphisms in Egytian deficient patients /  
 التحورات في الجين المسئول عن أنيميا الفول في المرضى المصريين 
Omnia Yahia Ibrahim Abdeldayem ; Supervised Hanaa Hamed Amaout , Nesrine Elgharbawi , Iman Abdelmohsen Abdushaheen 
 - Cairo :   Omnia Yahia Ibrahim Abdeldayem ,   2010 
 - 171 P. :   charts ;   25cm 
<br/><br/>Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology 
<br/><br/> Full molecular characterization of biochemical variants of glucose-6- phosphate dehydrogenase (G6PD) deficiency, using current techniques, is required as biochemical characterization has lost its significance as a means of identifying variants. In the present work, 50 G6PD deficient Egyptian children were subjected to quantitative G6PD enzyme assay 
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<br/><br/><label>Subjects--Index Terms: </label>ARMS G6PD deficiency Mediterrancan mutation