Case Reports
Dominant inherited familial factor VIII deficiency (Von Willebrand disease) associated with thrombocytopathic thrombocytopaenia. (Biologic and genetic implications)
- PMID: 4620093
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Case Reports
Dominant inherited familial factor VIII deficiency (Von Willebrand disease) associated with thrombocytopathic thrombocytopaenia. (Biologic and genetic implications)
Pathol Biol (Paris).
1974 Nov.
No abstract available
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