TY  - BOOK
AU  - Rania Srag Eldin Sayed
AU  - Heba Mahmoud Gouda , 
AU  - Iman Abdelmohsen Abdu Shaheen , 
AU  - Mona Salah Eldin Hamdy , 
TI  - Association of factor V leiden and prothrombin gene mutations with thrombotic risk in patients with sickle cell anemia / 
PY  - 2010///
CY  - Cairo : 
PB  - Rania Srag Eldin Sayed , 
KW  - Factor V Leiden
KW  - Prothrombin gene mutation
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 a group of genetic disorders of hemoglobin that causes multisystem morbidity and an increased risk of early death . Vascular complications are an important aspect of sick cell anemia although there is controversial evidence surrounding the role of thrombosis in the complication . Among the crucial inherited risk factors are factor V Leiden ( G1619A ) and prothrombin gene G20210A mutations
UR  - http://172.23.153.220/th.pdf
ER  -