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Gary D. Sinclair
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Journal Articles

Genomic instability after allogeneic hematopoietic cell transplantation is frequent in oral mucosa, particularly in patients with a history of chronic graft-versus-host disease, and rare in nasal mucosa

Brief Report
Faisal M. Khan, Sarah Sy, Polly Louie, Alejandra Ugarte-Torres, Noureddine Berka, Gary D. Sinclair, Douglas A. Stewart, James A. Russell, Jan Storek
Journal: Blood
Blood (2010) 116 (10): 1803–1806.
https://doi.org/10.1182/blood-2009-10-249201
Published: 2010
Includes: Supplemental data
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

Epithelial Cells of Donor Origin after Allogeneic HCT: Result of Cell Fusion, Transdifferentiation (plasticity) or Transfer of Epithelial Cell Precursors with the Graft?

Faisal Khan, PhD, Sarah Sy, Polly Louie, Megan Smith, Judy Chernos, Robyn Lee, Noureddine Berka, Gary D. Sinclair, Richard Leigh, David Proud, James A. Russell, Jan Storek, MD, PhD
Journal: Blood
Blood (2008) 112 (11): 387.
https://doi.org/10.1182/blood.V112.11.387.387
Published: 2008
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
Journal Articles

A novel type 2A von Willebrand factor mutation located at the last nucleotide of exon 26 (3538G>A) causes skipping of 2 nonadjacent exons

Paula D. James, Lee A. O'Brien, Carol A. Hegadorn, Colleen R. P. Notley, Gary D. Sinclair, Christine Hough, Man-Chiu Poon, David Lillicrap
Journal: Blood
Blood (2004) 104 (9): 2739–2745.
https://doi.org/10.1182/blood-2003-12-4286
Published: 2004