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Inherited Thrombophilia: Part 1
Thrombosis and Haemostasis · 1996 · Vol. 76(05) · pp. 651–662
David A. Lane✉(Charing Cross Hospital)Pier Mannuccio Mannucci(Ospedale Maggiore)Kenneth A. Bauer(Beth Israel Deaconess Hospital)Rogier M. Bertina(Leiden University)Nikolay P. Bochkov(Research Centre for Medical Genetics)Victor BoulyjnkovMammen Chandy(Christian Medical College)Björn Dahlbäck(Lund University)E. K. Ginter(Research Centre for Medical Genetics)Joseph P. Miletich(Washington University in St. Louis)Frits R. Rosendaal(Leiden University)Uri Seligsohn
Abstract
Based upon the World Health Organisation report of a Joint World Health Organisation/International Society on Thrombosis and Haemostasis Meeting held in Geneva, 6-8 November 1995. Published with permission of the World Health Organisation. Meeting Rapporteur; 2ISTH Secretariat, 6WHO Secretariat
Blood Coagulation and Thrombosis MechanismsHemophilia Treatment and ResearchCoagulation, Bradykinin, Polyphosphates, and AngioedemaMedicineThrombosisThrombophiliaFamily medicinePolitical scienceSurgery
MeSH terms
AnimalsDisease SusceptibilityEnzyme ActivationFactor V DeficiencyHumansRisk FactorsThrombosisIncidencePrevalenceProtein S DeficiencyProtein C DeficiencyAntithrombin III Deficiency
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References
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
Nature Genetics · 1995 · 5,697 citations
Inherited Antithrombin Deficiency Causing Thrombophilia
Thrombosis and Haemostasis · 1965 · 1,036 citations
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