Jackson SC, Sinclair GD, Cloutier S, Duan Z, Rand ML, Poon MC: The Montreal platelet syn-drome kindred has type 2B von Willebrand disease with the VWF V1316M mutation. Blood 113:3348-3351, 2009.
Wu J, Walker I, Clark D, Kahr WHA, Israels S, Rand ML, on behalf of the Rare Inherited Bleed-ing Disorders Sub-Committee of the Association of Hemophilia Clinic Directors of Canada: The Canadian Rare Inherited Bleeding Disorders Registry: Analysis of the first year of a national re-gistry of rare coagulation factor deficiencies and platelet disorders. Haemophilia 10 (Suppl 3):24-5, 2004. 26th International Congress of the World Federation of Hemophilia, Bangkok, Thailand, October 15-22, 2004.
Rand ML, Clark D, Walker I, Wu J: The Canadian Rare Inherited Bleeding Disorders Registry (RIBDR) of coagulation factor deficiencies and platelet function disorders. J Thromb Haemost 5 (Suppl 2):P-M-198, 2007. XXIst Congress of The International Society on Thrombosis and Haemostasis, Geneva, Switzerland, July 6-12, 2007.