TY  - BOOK
AU  - Othman Rizk Abdelmeguid Mishref
AU  - Nouran Fahmy Hussein , 
AU  - Shahira Amin Zayed , 
AU  - Zahraa Mohamed Ezz Eldeen , 
TI  - Gene mutation and qualitative enzyme assay of G٦PD enzyme deficiency in neonatal hyperbilirubinemia / 
PY  - 2013///
CY  - Cairo : 
PB  - Othman Rizk Abdelmeguid Mishref , 
KW  - G6PD deficiency
KW  - Mediterranean mutation
KW  - PCR-RFLP
N1  - Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Pediatrics; Issued also as CD
N2  - 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
UR  - http://172.23.153.220/th.pdf
ER  -