| 000 | 01959cam a2200349 a 4500 | ||
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| 003 | EG-GiCUC | ||
| 005 | 20250223030954.0 | ||
| 008 | 140415s2013 ua do f m 000 0 eng d | ||
| 040 |
_aEG-GiCUC _beng _cEG-GiCUC |
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| 041 | 0 | _aeng | |
| 049 | _aDeposite | ||
| 097 | _aPh.D | ||
| 099 | _aCai01.11.28.Ph.D.2013.Ot.G | ||
| 100 | 0 | _aOthman Rizk Abdelmeguid Mishref | |
| 245 | 1 | 0 |
_aGene mutation and qualitative enzyme assay of G٦PD enzyme deficiency in neonatal hyperbilirubinemia / _cOthman Rizk Abdelmeguid Mishref ; Supervised Zahraa Mohamed Ezz Eldeen , Shahira Amin Zayed , Nouran Fahmy Hussein |
| 246 | 1 | 5 | _aالتحور الجينى و الكشف الكيفى لنقص إنزيم جلوكوز٦فوسفات الهيدروجين فى الأطفال حديثى الولادة الذين يعانون من صفراء بالدم |
| 260 |
_aCairo : _bOthman Rizk Abdelmeguid Mishref , _c2013 |
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| 300 |
_a158 P. : _bcharts , photographs ; _c25cm |
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| 502 | _aThesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Pediatrics | ||
| 520 | _aMolecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency variants is essential, especially since the biochemical characterization has lost its significance due to the individual variability. As a result, cases can be misdiagnosed. The present study was designed to determine the incidence of G6PD mediterranean (Med) mutation among Egyptian children with G6PD deficiency as well as its molecular association with the G6PD 1311T silent polymorphism | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _aG6PD deficiency | |
| 653 | 4 | _aMediterranean mutation | |
| 653 | 4 | _aPCR-RFLP | |
| 700 | 0 |
_aNouran Fahmy Hussein , _eSupervisor |
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| 700 | 0 |
_aShahira Amin Zayed , _eSupervisor |
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| 700 | 0 |
_aZahraa Mohamed Ezz Eldeen , _eSupervisor |
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| 856 | _uhttp://172.23.153.220/th.pdf | ||
| 905 |
_aNazla _eRevisor |
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| 905 |
_aSamia _eCataloger |
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| 942 |
_2ddc _cTH |
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| 999 |
_c45782 _d45782 |
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