Gene mutation and qualitative enzyme assay of G٦PD enzyme deficiency in neonatal hyperbilirubinemia / Othman Rizk Abdelmeguid Mishref ; Supervised Zahraa Mohamed Ezz Eldeen , Shahira Amin Zayed , Nouran Fahmy Hussein

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Othman Rizk Abdelmeguid Mishref

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TextLanguage: English Publication details: Cairo : Othman Rizk Abdelmeguid Mishref , 2013Description: 158 P. : charts , photographs ; 25cmOther title:

التحور الجينى و الكشف الكيفى لنقص إنزيم جلوكوز٦فوسفات الهيدروجين فى الأطفال حديثى الولادة الذين يعانون من صفراء بالدم [Added title page title]

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Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Pediatrics Summary: Molecular 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

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Item type	Current library	Home library	Call number	Copy number	Status	Barcode
Thesis	قاعة الرسائل الجامعية - الدور الاول	المكتبة المركزبة الجديدة - جامعة القاهرة	Cai01.11.28.Ph.D.2013.Ot.G (Browse shelf(Opens below))		Not for loan	01010110062432000
CD - Rom	مخـــزن الرســائل الجـــامعية - البدروم	المكتبة المركزبة الجديدة - جامعة القاهرة	Cai01.11.28.Ph.D.2013.Ot.G (Browse shelf(Opens below))	62432.CD	Not for loan	01020110062432000

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Previous	Cai01.11.28.Ph.D.2013.Na.F Fecal calprotectin : A non - invasive screening test for inflammatory bowel disease among Egyptian children with colitis /	Cai01.11.28.Ph.D.2013.Ne.E The effect of glutathione-S-Transferase (GST) genes polymorphisms on the phenotypic expression of asthma in Egyptian children /	Cai01.11.28.Ph.D.2013.Ne.E The effect of glutathione-S-Transferase (GST) genes polymorphisms on the phenotypic expression of asthma in Egyptian children /	Cai01.11.28.Ph.D.2013.Ot.G Gene mutation and qualitative enzyme assay of G٦PD enzyme deficiency in neonatal hyperbilirubinemia /	Cai01.11.28.Ph.D.2013.Ot.G Gene mutation and qualitative enzyme assay of G٦PD enzyme deficiency in neonatal hyperbilirubinemia /	Cai01.11.28.Ph.D.2013.Ra.N Nesfin-1 concentration in obese children and young adolescents and its relation to body composition and dietary intake /	Cai01.11.28.Ph.D.2013.Ra.N Nesfin-1 concentration in obese children and young adolescents and its relation to body composition and dietary intake /	Next

Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Pediatrics

Molecular 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

Issued also as CD

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