Maternal and off-spring Methylenetetrahydrofolate reductase gene C677T polymorphism Does it influence the prevalence of congenital heart defects in Egyptian neonates? / Nouran Farouk Elnaggar ; Supervised Reem Nabil Said , Dina Mohamed Elabd , Baher Matta N. Hanna
Material type:
- التنوع الجينى لانزيم الميثلين تتراهيدروفولات ريداكتاز لدى الامهات واطفالهم ؛ هل يؤثر على مدى حدوث العيوب الخلقية بالقلب لدى الرضع المصريين؟ [Added title page title]
- Issued also as CD
Item type | Current library | Home library | Call number | Copy number | Status | Barcode | |
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.28.M.Sc.2011.No.M (Browse shelf(Opens below)) | Not for loan | 01010110056494000 | ||
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.28.M.Sc.2011.No.M (Browse shelf(Opens below)) | 56494.CD | Not for loan | 01020110056494000 |
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Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Pediatrics
Congenital heart defects (CHDs) are the most prevalent heart disease in neonates . There is evidence suggesting that the risk of CHDs may be related to maternal folate status as well as genetic variants in folate - related genes . Aim of work : I nvestigating the relation between MTHFR C677T gene polymorphism and CHDs in full - term neonates and considering the possible role of folate supplementation in the prevention of CHDs
Issued also as CD
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