The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort study von James, Paula D., Notley, Colleen, Hegadorn, Carol, Leggo, Jayne, Tuttle, Angie, Tinlin, Shawn, Brown, Christine, Andrews, Chandler, Labelle, Andrea, Chirinian, Yvette, O'Brien, Lee, Othman, Maha, Rivard, Georges, Rapson, Dilys, Hough, Christine, Lillicrap, David

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The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort study von James, P. D., Notley, C., Hegadorn, C., Leggo, J., Tuttle, A., Tinlin, S., Brown, C., Andrews, C., Labelle, A., Chirinian, Y., O'Brien, L., Othman, M., Rivard, G., Rapson, D., Hough, C., Lillicrap, D.

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Functional characterization of a 13-bp deletion (c.-1522_-1510del13) in the promoter of the von Willebrand factor gene in type 1 von Willebrand disease von Othman, Maha, Chirinian, Yvette, Brown, Christine, Notley, Colleen, Hickson, Nicholas, Hampshire, Daniel, Buckley, Suzanne, Waddington, Simon, Parker, Alan L., Baker, Andrew, James, Paula, Lillicrap, David

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In Vitro and In Vivo Mouse Models of the Type 1 Von Willebrand Disease Mutations Y1584C and R1205H von Pruss, Cynthia M., Sponagle, Kate, Laverty, Kimberly, Hegadorn, Carol A., Chirinian, Yvette, Notley, Colleen, Golder, Mia, Lillicrap, David

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The mutational spectrum of type 1 von Willebrand disease : results from a Canadian cohort study. Commentary von SADLER, J. Evan, JAMES, Paula D, CHIRINIAN, Yvette, O'BRIEN, Lee, OTHMAN, Maha, RIVARD, Georges, RAPSON, Dilys, HOUGH, Christine, LILLICRAP, David, NOTLEY, Colleen, HEGADORN, Carol, LEGGO, Jayne, TUTTLE, Angie, TINLIN, Shawn, BROWN, Christine, ANDREWS, Chandler, LABELLE, Andrea

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