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Q33823350-50C6779F-0117-46AE-9B73-EE568C279C52
Q33823350-50C6779F-0117-46AE-9B73-EE568C279C52
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33823350-50C6779F-0117-46AE-9B73-EE568C279C52
Editorial: The hemophiloid diseases and factor VIII. Clinical molecular biology
P2860
Q33823350-50C6779F-0117-46AE-9B73-EE568C279C52
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33823350-50C6779F-0117-46AE-9B73-EE568C279C52
rank
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type
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Statement
wasDerivedFrom
675ad31ab8a3149819f3df5e7674f46b2a391b89
P2860
Immunologic differentiation of classic hemophilia (factor 8 deficiency) and von Willebrand's dissase, with observations on combined deficiencies of antihemophilic factor and proaccelerin (factor V) and on an acquired circulating anticoagulant agains