TY  - BOOK
AU  - Yasmine Mohamed Amrousy
AU  - Menat Allah Kamal Eldeen , 
AU  - Mervat Mamdouh Khorshied , 
AU  - Zainab Ali Hassan Elsadani , 
TI  - Mannose binding lectin (MBL2) gene variants in siekle cell disease / 
PY  - 2011///
CY  - Cairo : 
PB  - Yasmine Mohamed Amrousy , 
KW  - MBL2
KW  - Polymorphism
KW  - Sickle cell disease
N1  - Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology; Issued also as CD
N2  - 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
UR  - http://172.23.153.220/th.pdf
ER  -