Linkage of combined factors V and VIII deficiency to chromosome 18q by homozygosity mapping.

Por Nichols, W C, Seligsohn, U, Zivelin, A, Terry, V H, Arnold, N D, Siemieniak, D R, Kaufman, R J, Ginsburg, D
Publicado em 1997

Genome-wide studies of von Willebrand Factor Propeptide Identify Loci Contributing to Variation in Propeptide Levels and von Willebrand Factor Clearance

Por Ozel, A.B., McGee, B., Siemieniak, D., Jacobi, P.M., Haberichter, S.L., Brody, L.C., Mills, J.L., Molloy, A.M., Ginsburg, D., Li, J.Z., Desch, K.C.
Publicado no J Thromb Haemost (2016)