Pages that link to "Q34152374"
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The following pages link to Factor V Leiden thrombophilia (Q34152374):
Displaying 50 items.
- Phased whole-genome genetic risk in a family quartet using a major allele reference sequence (Q21144940) (← links)
- Venous thromboembolism and sarcoidosis: co-incidence or coexistence? (Q26767140) (← links)
- Progress in research into the genes associated with venous thromboembolism (Q28084640) (← links)
- The phenotypic legacy of admixture between modern humans and Neandertals (Q28603615) (← links)
- Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network (Q28673413) (← links)
- The role of FV 1691G>A, FII 20210G>A mutations and MTHFR 677C>T; 1298A>C and 103G>T FXIII gene polymorphisms in pathogenesis of intraventricular hemorrhage in infants born before 32 weeks of gestation (Q33871030) (← links)
- Management of inherited thrombophilia: guide for genetics professionals (Q34195599) (← links)
- Prevalence of 1691G>A FV mutation in females from Bosnia and Herzegovina--a preliminary report. (Q35099729) (← links)
- Prevalence of 1691G>A FV mutation in Poland compared with that in other Central, Eastern and South-Eastern European countries (Q35184397) (← links)
- Atrial Fibrillation in the Young: A Neurologist's Nightmare (Q35438395) (← links)
- ELISA-Based Detection System for Protein S K196E Mutation, a Genetic Risk Factor for Venous Thromboembolism (Q35694527) (← links)
- Right Ventricular Thrombus in a 36-Year-Old Man with Factor V Leiden (Q35827440) (← links)
- Phenome-Wide Association Study to Explore Relationships between Immune System Related Genetic Loci and Complex Traits and Diseases (Q36100091) (← links)
- Small bowel varices secondary to chronic superior mesenteric vein thrombosis in a patient with heterozygous Factor V Leiden mutation: a case report (Q36110133) (← links)
- Atherosclerotic and thrombotic genetic and environmental determinants in Egyptian coronary artery disease patients: a pilot study. (Q36249248) (← links)
- Exacerbated venous thromboembolism in mice carrying a protein S K196E mutation (Q36253998) (← links)
- Prevalence and role of antithrombin III, protein C and protein S deficiencies and activated protein C resistance in Kosovo women with recurrent pregnancy loss during the first trimester of pregnancy (Q36406584) (← links)
- Recurrent pregnancy loss in a subject with heterozygote factor V Leiden mutation; a case report (Q36589500) (← links)
- Highly specific SNP detection using 2D graphene electronics and DNA strand displacement (Q37065217) (← links)
- Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease (Q37187461) (← links)
- A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders (Q37243310) (← links)
- Allele frequency distribution of 1691G >A F5 (which confers Factor V Leiden) across Europe, including Slavic populations (Q37301084) (← links)
- Joint effects of cancer and variants in the factor 5 gene on the risk of venous thromboembolism (Q37331210) (← links)
- Patient compliance based on genetic medicine: a literature review. (Q37471829) (← links)
- Management of inherited thrombophilia in pregnancy (Q37730086) (← links)
- Etiopathogenesis of Sheehan's Syndrome: Roles of Coagulation Factors and TNF-Alpha (Q37730732) (← links)
- Recurrent venous thromboembolism in a patient with heterozygous factor v leiden mutation (Q38283515) (← links)
- Fatal pulmonary embolism following ultrasound-guided foam sclerotherapy combined with multiple microphlebectomies (Q38580591) (← links)
- Thrombosis of a descending thoracic aortic endovascular stent graft in a patient with factor V Leiden: case report (Q38722709) (← links)
- Polymorphisms of the coagulation system and risk of cancer (Q38805421) (← links)
- Electronic health record interventions at the point of care improve documentation of care processes and decrease orders for genetic tests commonly ordered by nongeneticists. (Q38881922) (← links)
- Impact of Prothrombotic Risk Factors in a Cohort of Egyptian Hemophilia A Patients (Q38986880) (← links)
- Diagnosis and management of factor V Leiden. (Q38994953) (← links)
- Genetic, hematological, and immunological disorders transmissible with liver transplantation (Q39152643) (← links)
- Economic Evaluations of Thrombophilia Screening Prior to Prescribing Combined Oral Contraceptives: A Systematic and Critical Review. (Q39177130) (← links)
- Gastrointestinal bleeding in patients on novel oral anticoagulants: Risk, prevention and management. (Q39217774) (← links)
- Genetic Risk Factors of Venous Thromboembolism in the East Algerian Population (Q39276259) (← links)
- Collaborative Counseling Considerations for Pharmacogenomic Tests (Q39411218) (← links)
- Prevalence of common hereditary risk factors for thrombophilia in Somalia and identification of a novel Gln544Arg mutation in coagulation factor V. (Q40049106) (← links)
- Rs5918ITGB3 Polymorphism, Smoking, and BMI as Risk Factors for Early Onset and Recurrence of DVT in Young Women (Q40135109) (← links)
- Genetic Risk Factors in Venous Thromboembolism. (Q40577579) (← links)
- Factor V Leiden and Cardiopulmonary Bypass (Q42057735) (← links)
- Novel genes and mutations in patients affected by recurrent pregnancy loss. (Q42706616) (← links)
- Thrombosis after liver transplantation for hepatocellular carcinoma (Q43026378) (← links)
- A risk-benefit analysis of factor V Leiden testing to improve pregnancy outcomes: a case study of the capabilities of decision modeling in genomics (Q46321924) (← links)
- Genetic markers for inherited thrombophilia are associated with fetal growth retardation in the population of Central Russia. (Q48094342) (← links)
- Necessity and risks of arterial blood sampling in healthy volunteer studies (Q48127644) (← links)
- Cerebral sinus venous thrombosis during childhood acute lymphoblastic leukemia therapy: Risk factors and management. (Q48204205) (← links)
- Are the gene-patent storm clouds dissipating? A global snapshot (Q48205224) (← links)
- PlA2 Polymorphism in Glycoprotein IIb/IIIa Modulates the Morphology and Nanomechanics of Platelets. (Q51047838) (← links)