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Clinical Laboratory Science : Journal of the American Society for Medical Technology
|
June 5, 2003
Hereditary deficiencies of antithrombin III, protein S, and the protein C pathway in Jordanian thrombosis patients
Suhair S Eid
Clinical Laboratory Science : Journal of the American Society for Medical Technology
|
November 24, 2004
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians
Suhair S Eid, Ghada Rihani
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
August 12, 2005
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR G677A among 594 thrombotic Jordanian patients
Suhair S Eid, Taisir Shubeilat
Clinical Laboratory Science : Journal of the American Society for Medical Technology
|
January 30, 2009
Inherited bleeding disorders: a 14-year retrospective study
Suhair S Eid, Nazmi R Kamal, Taisir S Shubeilat, et al.
Human Reproduction (Oxford, England)
|
July 13, 2006
Acquired and inherited thrombophilia: implication in recurrent IVF and embryo transfer failure
Hussein S Qublan, Suhair S Eid, Hani A Ababneh, et al.
European Journal of Haematology
|
January 17, 2016
Thrombophilic risk of individuals with rare compound factor V Leiden and prothrombin G20210A polymorphisms: an international case series of 100 individuals
Ming Y Lim, Allison M Deal, Steven Kim, et al.
Human Mutation
|
October 8, 2009
Widening the mutation spectrum of EVC and EVC2: ectopic expression of Weyer variants in NIH 3T3 fibroblasts disrupts Hedgehog signaling
Maria Valencia, Pablo Lapunzina, Derek Lim, et al.
European Journal of Epidemiology
|
August 1, 2013
Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls
Benedetto Simone, Valerio De Stefano, Emanuele Leoncini, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Clinical Laboratory Science : Journal of the American Society for Medical Technology
|
June 5, 2003
Hereditary deficiencies of antithrombin III, protein S, and the protein C pathway in Jordanian thrombosis patients
Suhair S Eid
Clinical Laboratory Science : Journal of the American Society for Medical Technology
|
November 24, 2004
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians
Suhair S Eid, Ghada Rihani
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
August 12, 2005
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR G677A among 594 thrombotic Jordanian patients
Suhair S Eid, Taisir Shubeilat
Clinical Laboratory Science : Journal of the American Society for Medical Technology
|
January 30, 2009
Inherited bleeding disorders: a 14-year retrospective study
Suhair S Eid, Nazmi R Kamal, Taisir S Shubeilat, et al.
Human Reproduction (Oxford, England)
|
July 13, 2006
Acquired and inherited thrombophilia: implication in recurrent IVF and embryo transfer failure
Hussein S Qublan, Suhair S Eid, Hani A Ababneh, et al.
European Journal of Haematology
|
January 17, 2016
Thrombophilic risk of individuals with rare compound factor V Leiden and prothrombin G20210A polymorphisms: an international case series of 100 individuals
Ming Y Lim, Allison M Deal, Steven Kim, et al.
Human Mutation
|
October 8, 2009
Widening the mutation spectrum of EVC and EVC2: ectopic expression of Weyer variants in NIH 3T3 fibroblasts disrupts Hedgehog signaling
Maria Valencia, Pablo Lapunzina, Derek Lim, et al.
European Journal of Epidemiology
|
August 1, 2013
Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls
Benedetto Simone, Valerio De Stefano, Emanuele Leoncini, et al.
Page
of 1