American College of Medical Genetics consensus statement on factor V Leiden mutation testing - Test2 - elhamkhani - TriplyDB

American College of Medical Genetics consensus statement on factor V Leiden mutation testing

American College of Medical Genetics consensus statement on factor V Leiden mutation testing

http://www.wikidata.org/entity/Q28361651

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Keeping up with the next generation: massively parallel sequencing in clinical diagnostics Beta-synuclein gene alterations in dementia with Lewy bodies.Guidance for the evaluation and treatment of hereditary and acquired thrombophilia Patients' understanding of genetic susceptibility testing in mainstream medicine: qualitative study on thrombophilia Replication and characterisation of genetic variants in the fibrinogen gene cluster with plasma fibrinogen levels and haematological traits in the Third National Health and Nutrition Examination Survey Testing for hereditary thrombophilia: a retrospective analysis of testing referred to a national laboratory.The importance of homozygous polymorphisms of methylenetetrahydrofolate reductase gene in romanian patients with idiopathic venous thromboembolism.Factor V Leiden thrombophilia.ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing.Usefulness of factor V Leiden mutation testing in clinical practice.Factor V Leiden, prothrombin G20210A substitution and hormone therapy: indications for molecular screening.Commercial molecular diagnostics in the U.S.: The Human Genome Project to the clinical laboratory.Genetic diagnosis and testing in clinical practice Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium.The genetic family history as a risk assessment tool in internal medicine.Use of Factor V Leiden genetic testing in practice and impact on management Role of the geneticist in testing and counseling for inherited thrombophilia.Development and integration of molecular genetic tests into clinical practice: the US experience.Utility of testing for factor V Leiden.Futility of testing for factor V Leiden Factor V Leiden as a common genetic risk factor for venous thromboembolism.Recurrent pregnancy loss in a subject with heterozygote factor V Leiden mutation; a case report The Frequency of Some Thrombophilic Mutations in Eastern Turkey.Pharmacogenetic typing for oral anti-coagulant response among factor V Leiden mutation carriers.Motivating factors for physician ordering of factor V Leiden genetic tests Genetic variations and their influence on risk and treatment of venous thrombosis.The Obstetric Medicine Listserv: review of controversies surrounding thrombophilia testing Laboratory informatics based evaluation of methylene tetrahydrofolate reductase C677T genetic test overutilization.Health-related direct-to-consumer genetic tests: a public health assessment and analysis of practices related to Internet-based tests for risk of thrombosis.Role of thrombophilia testing: con.Economic Evaluations of Thrombophilia Screening Prior to Prescribing Combined Oral Contraceptives: A Systematic and Critical Review.Genetic Risk Factors in Venous Thromboembolism.Cystic fibrosis testing comes of age.Factor V Leiden: to test or not to test, that is the debate.Who should be tested for thrombophilia?A curated gene list for reporting results of newborn genomic sequencing.Can haematological tests predict cardiovascular risk? The 2005 Kettle Lecture.Expanded carrier screening and the law of unintended consequences: from cystic fibrosis to fragile X.The Evaluation of Serum Copeptin Levels and Some Commonly Seen Thrombophilic Mutation Prevalence in Acute Pulmonary Embolism.Family history unawareness of blood clot risk: links to misdiagnoses and illness uncertainties in personal and expert realms.

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American College of Medical Genetics consensus statement on factor V Leiden mutation testing

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P2860

Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C

Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study

The mechanism of inactivation of human factor V and human factor Va by activated protein C

The lupus anticoagulant/antiphospholipid syndrome.

Heritable coagulopathies in pregnancy.

Inherited thrombophilia and pregnancy loss.

Predictors of recurrence after deep vein thrombosis and pulmonary embolism: a population-based cohort study.

The factor V Leiden mutation may predispose women to severe preeclampsia.

A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.

Ethnic distribution of factor V Leiden in 4047 men and women. Implications for venous thromboembolism screening.

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