Cooney, K. A., Nichols, W. C., Bruck, M. E., Bahou, W. F., Shapiro, A. D., Bowie, E. J., . . . Ginsburg, D. (1991). The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding domain.

Cooney, K A., W C. Nichols, M E. Bruck, W F. Bahou, A D. Shapiro, E J. Bowie, H R. Gralnick, e D. Ginsburg. The Molecular Defect in Type IIB Von Willebrand Disease. Identification of Four Potential Missense Mutations Within the Putative GpIb Binding Domain. 1991.

Cooney, K A., et al. The Molecular Defect in Type IIB Von Willebrand Disease. Identification of Four Potential Missense Mutations Within the Putative GpIb Binding Domain. 1991.