Associated a - thalassaemia as an ameliorating factor in homozygous B - thalassaemia / Nada Mohamed Fadel ; Supervised Normeen Kaddah , Samia Rizk , Ahmed Maher
Language: Eng Publication details: Cairo : Nada Mohamed Fadel , 2006Description: 159P : ill ; 30cmOther title:- تاثيراختفاء المورثة الالفية على الحالة الاكلينيكية لمرضى انيميا البحر الابيض المتوسط البائية الوسطية [Added title page title]
- Issued also as CD
Item type | Current library | Home library | Call number | Status | Date due | Barcode | |
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Thesis | قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.28.Ph.D.2006.Na.A. (Browse shelf(Opens below)) | Not for loan | 01010110046202000 | ||
CD - Rom | مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.28.Ph.D.2006.Na.A. (Browse shelf(Opens below)) | Not for loan | 01020110046202000 |
Thesis (PH.D.) - Cairo University - Faculty Of Medicine - Department Of Pediatrics
The main determinant of the severity of ? - thalassemia is the degree of globin chain imbalanceCoinheritance of ? - thalassaemia ameliorate the clinical presentationThis study included 22 patients (10 males and 22 females) They were diagnosed on clinical basis as ? - thalassaemia intermedia patients
Issued also as CD
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