Mannose binding lectin (MBL2) gene variants in siekle cell disease / Yasmine Mohamed Amrousy ; Supervised Menat Allah Kamal Eldeen , Mervat Mamdouh Khorshied , Zainab Ali Hassan Elsadani

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Yasmine Mohamed Amrousy

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TextLanguage: English Publication details: Cairo : Yasmine Mohamed Amrousy , 2011Description: 113 P. : charts ; 25cmOther title:

التعدد الجيني لجين المانوز الرابط اللكتيني في مرض أنيميا الخلايا المنجلية [Added title page title]

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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology Summary: Sickle cell disease (SCD) is an inherited disorder of sickle hemoglobin affecting millions of people wordwide. The current study aimed at detecting the prevalence of MBL2 exon-1 (codon 52, 54 and 57) and promoter region (-221, X/Y) genetic polymorphisms in Egyptian children with SCD to clear out its possible role as a genetic risk factor for susceptibility to venous occlusion (VOC) and/or infections

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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	Cai01.11.07.M.Sc.2011.Ya.M (Browse shelf(Opens below))		Not for loan	01010110056727000
CD - Rom	مخـــزن الرســائل الجـــامعية - البدروم	المكتبة المركزبة الجديدة - جامعة القاهرة	Cai01.11.07.M.Sc.2011.Ya.M (Browse shelf(Opens below))	56727.CD	Not for loan	01020110056727000

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Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology

Sickle cell disease (SCD) is an inherited disorder of sickle hemoglobin affecting millions of people wordwide. The current study aimed at detecting the prevalence of MBL2 exon-1 (codon 52, 54 and 57) and promoter region (-221, X/Y) genetic polymorphisms in Egyptian children with SCD to clear out its possible role as a genetic risk factor for susceptibility to venous occlusion (VOC) and/or infections

Issued also as CD

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