Molecular genetic study of Egyptian hereditary spherocytosis patients with combined ankyrin spectrin deficiency / Heba Mohamed Hassan Ahmed Abouelew ; Supervised Azza Mostafa , Samia Hassan Rizk , Amal Elbehlawy
Language: Eng Publication details: Cairo : Heba Mohamed Hassan Ahmed Abouelew , 2001Description: 103P. ; 25cmOther title:- دراسة جزيئية للمرضى المصريين المصابين بمرض تكور خلايا الدم الحمراء الوراثى الذين يعانون من نقص مركب فى الانكرين والسبكترين [Added title page title]
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.07.Ph.D.2001.He.M (Browse shelf(Opens below)) | Not for loan | 01010110036543000 |
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Cai01.11.07.Ph.D.2001.Ay.R Relevance of factor V leiden in patients with recurrent spontaneous abortions / | Cai01.11.07.Ph.D.2001.Ay.R Relevance of factor V leiden in patients with recurrent spontaneous abortions / | Cai01.11.07.Ph.D.2001.Az.E Effect of leucofiltration on prevention of transfusion - acquired cytomegalovirus infection / | Cai01.11.07.Ph.D.2001.He.M Molecular genetic study of Egyptian hereditary spherocytosis patients with combined ankyrin spectrin deficiency / | Cai01.11.07.Ph.D.2001.Ma.D Detection of genital herpes simplex virus by isolation and serological assay / | Cai01.11.07.Ph.D.2001.Ma.D Detection of genital herpes simplex virus by isolation and serological assay / | Cai01.11.07.Ph.D.2001.Ma.R Role of cytomegalovirus in renal transplant patients / |
Thesis (Ph.D.) - Cairo University - Faculty Of Medicine - Department Of Clinical and Chemical Pathology
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