International Society on Thrombosis and Haemostasis

Home | Membership | Contact Us
JTH Editors' Page | JTH Online | JTH Homepage | Manuscript Central | Editors Information
Officers | Scientific Subcommittees | Senior Advisory Council | Official Communications | Bibliography | Working Group/Liaison Reports
Official Communications | SSC Minutes and Reports | Abstracts | Monographs
SSC Registries | Other Registries
ISTH-WHO Standards | SSC Working Group on Coagulation Standards
SSC Member's Only | Council Member's Only
Societies and Associations | Journals | Resources | Meetings

Other Registries/Databases:

Antiphospholipid Syndrome Collaborative Registry (APSCORE)

Factor VII Mutation Database

Factor VIII Database

Fibrinogen Database

Human Gene Mutation Database

Mutations causing rare bleeding disorders: (deficiencies of prothrombin, factor V, factor VII, factor X, factor XI, factor XIII: A and B, and combined factor V and VIII). UPDATED TO FEBRUARY 15, 2007
Supplement to Chapter 116 of Williams Hematology 7 th Edition 2006 (printed with permission from McGraw Hill)

Protein C Database

About the ISTH | Site Map | Privacy Policy | © 2007 International Society on Thrombosis and Haemostasis