Seminars in Thrombosis and Hemostasis
Issue 06 · September 2008
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485
Othman, Maha:
Molecular Genetic Testing in Hemostasis and Thrombosis: The Past, the Present, and the Future
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491
Goodeve, Anne:
Molecular Genetic Testing of Hemophilia A
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502
James, Paula; Lillicrap, David:
The Role of Molecular Genetics in Diagnosing von Willebrand Disease
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509
Novelli, Enrico M.; Ragni, Margaret V.:
Genetics of Bleeding Disorders in Women
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520
Othman, Maha; Favaloro, Emmanuel J.:
Genetics of type 2B von Willebrand Disease: “True 2B,”“tricky 2B,” or “Not 2B.” What Are the Modifiers of the Phenotype?
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532
Senzel, Lisa; Gnatenko, Dmitri V.; Bahou, Wadie F.:
Genomic and Proteomic Applications in Diagnosis of Platelet Disorders and Classification
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539
Curtis, Brian R.:
Genotyping for Human Platelet Alloantigen Polymorphisms: Applications in the Diagnosis of Alloimmune Platelet Disorders
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549
Varga, Elizabeth A.; Kerlin, Bryce A.; Wurster, Mark W.:
Social and Ethical Controversies in Thrombophilia Testing and Update on Genetic Risk Factors for Venous Thromboembolism
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562
Asselbergs, Folkert W.; Pattin, Kristine; Snieder, Harold; Hillege, Hans L.; van Gilst, Wiek H.; Moore, Jason H.:
Genetic Architecture of Tissue-Type Plasminogen Activator and Plasminogen Activator Inhibitor-1
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569
Ozelo, Margareth Castro; Zapata Esp., Roman; Qadura, Mohammad; Chegeni, Rouzbeh; Othman, Maha:
Molecular Genetic Testing of Hemostasis and Thrombosis in Developing Countries: Achievements, Hopes, and Challenges
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