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Journal Articles

The Montreal platelet syndrome kindred has type 2B von Willebrand disease with the VWF V1316M mutation

Brief Report
Shannon C. Jackson, Gary D. Sinclair, Stephanie Cloutier, Zhaoxia Duan, Margaret L. Rand, Man-Chiu Poon
Journal: Blood
Blood (2009) 113 (14): 3348–3351.
https://doi.org/10.1182/blood-2008-06-165233
Published: 2009
Journal Articles

Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy

Carolyn J. Owen, Cynthia L. Toze, Anna Koochin, Donna L. Forrest, Clayton A. Smith, Jane M. Stevens, Shannon C. Jackson, Man-Chiu Poon, Gary D. Sinclair, Brian Leber, Peter R. E. Johnson, Anthony Macheta, John A. L. Yin, Michael J. Barnett, T. Andrew Lister, Jude Fitzgibbon
Journal: Blood
Blood (2008) 112 (12): 4639–4645.
https://doi.org/10.1182/blood-2008-05-156745
Published: 2008
Includes: Supplemental data
Journal Articles

Five New Pedigrees with Inherited RUNX1 Mutations Causing Familial Platelet Disorder with Propensity to Myeloid Malignancy (FPD/AML)

Carolyn J Owen, Cynthia L Toze, Anna Koochin, Donna L. Forrest, Clayton A. Smith, Shannon C Jackson, Man-Chiu Poon, Gary D. Sinclair, Brian Leber, Peter Johnson, Anthony Macheta, John AL Yin, Michael J. Barnett, T. Andrew Lister, Jude Fitzgibbon
Journal: Blood
Blood (2008) 112 (11): 5067.
https://doi.org/10.1182/blood.V112.11.5067.5067
Published: 2008