| 000 | 01688cam a2200349 a 4500 | ||
|---|---|---|---|
| 003 | EG-GiCUC | ||
| 005 | 20250223030258.0 | ||
| 008 | 100921s2010 ua d f m 000 0 eng d | ||
| 040 |
_aEG-GiCUC _beng _cEG-GiCUC |
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| 041 | 0 | _aeng | |
| 049 | _aDeposite | ||
| 097 | _aM.Sc | ||
| 099 | _aCai01.11.07.M.Sc.2010.Om.G | ||
| 100 | 0 | _aOmnia Yahia Ibrahim Abdeldayem | |
| 245 | 1 | 0 |
_aG6PD gene polymorphisms in Egytian deficient patients / _cOmnia Yahia Ibrahim Abdeldayem ; Supervised Hanaa Hamed Amaout , Nesrine Elgharbawi , Iman Abdelmohsen Abdushaheen |
| 246 | 1 | 5 | _aالتحورات في الجين المسئول عن أنيميا الفول في المرضى المصريين |
| 260 |
_aCairo : _bOmnia Yahia Ibrahim Abdeldayem , _c2010 |
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| 300 |
_a171 P. : _bcharts ; _c25cm |
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| 502 | _aThesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology | ||
| 520 | _aFull 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 | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _aARMS | |
| 653 | 4 | _aG6PD deficiency | |
| 653 | 4 | _aMediterrancan mutation | |
| 700 | 0 |
_aHanaa Hamed Amaout , _eSupervisor |
|
| 700 | 0 |
_aIman Abdelmohsen Abdushaheen , _eSupervisor |
|
| 700 | 0 |
_aNesrine Elgharbawi , _eSupervisor |
|
| 856 | _uhttp://172.23.153.220/th.pdf | ||
| 905 |
_aMustafa _eRevisor |
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| 905 |
_aSamia _eCataloger |
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| 942 |
_2ddc _cTH |
||
| 999 |
_c31409 _d31409 |
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