RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164087682 T1 von Willebrand-Jürgens Disease T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164087682 RD 2024/04/24 AB A hereditary family of blood-clotting disorders caused by a deficiency of the von Willebrand factor protein and factor VIII protein, and characterized by prolonged bleeding.