Donors with a rare pheno (geno) type
Reesink, H. W., Engelfriet, C. P., Schennach, H., Gassner, C., Wendel, S., Fontão-Wendel, R., De Brito, M. A., Sistonen, P., Matilainen, J., Peyrard, T., Pham, B. N., Rouger, P., Le Pennec, P. Y., Flegel, W. A., Von Zabern, I., Lin, C. K., Tsoi, W. C., Hoffer, I., Barotine-Toth, K., Joshi, S. R., Vasantha, K., Yahalom, V., Asher, O., Levene, C., Villa, M. A., Revelli, N., Greppi, N., Marconi, M., Tani, Y., Folman, C. C., De Haas, M., Koopman, M. M. W., Beckers, E., Gounder, D. S., Flanagan, P., Wall, L., Aranburu Urtasun, E., Hustinx, H., Niederhauser, C., Flickinger, C., Nance, S. J., Meny, G. M.
Published in Vox sanguinis (01.10.2008)
Published in Vox sanguinis (01.10.2008)
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Journal Article
Clinical manifestations of the thrombocytopenia and absent radii (TAR) syndrome
Gounder, D S, Pullon, H W, Ockelford, P A, Nicol, R O
Published in Australian and New Zealand journal of medicine (01.10.1989)
Published in Australian and New Zealand journal of medicine (01.10.1989)
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Journal Article