DNA-based mutation analysis of Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinaemia. by Vorechovský, I, Vihinen, M, de Saint Basile, G, Honsová, S, Hammarström, L, Müller, S, Nilsson, L, Fischer, A, Smith, C

CD40lbase: a database of CD40L gene mutations causing X-linked hyper-IgM syndrome. by Notarangelo, L, Peitsch, M, Abrahamsen, T, Bachelot, C, Bordigoni, P, Cant, A, Chapel, H, Clementi, M, Deacock, S, de Saint Basile, G, Duse, M, Espanol, T, Etzioni, A, Fasth, A, Fischer, A, Giliani, S, Gomez, L, Hammarstorm, L, Jones, A, Kanariou, M, Kinnon, C, Klemola, T, Kroczek, R, Levy, J, Matamoros, N

X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease. by Booth, C, Gilmour, K, Veys, P, Gennery, A, Slatter, M, Chapel, H, Heath, P, Steward, C, Smith, O, O'Meara, A, Kerrigan, H, Mahlaoui, N, Cavazzana-Calvo, M, Fischer, A, Moshous, D, Blanche, S, Pachlopnik Schmid, J, Latour, S, de Saint-Basile, G, Albert, M, Notheis, G, Rieber, N, Strahm, B, Ritterbusch, H, Lankester, A

LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1. by Hacein-Bey-Abina, S, Von Kalle, C, Schmidt, M, McCormack, M, Wulffraat, N, Leboulch, P, Lim, A, Osborne, C, Pawliuk, R, Morillon, E, Sorensen, R, Forster, A, Fraser, P, Cohen, J, de Saint Basile, G, Alexander, I, Wintergerst, U, Frebourg, T, Aurias, A, Stoppa-Lyonnet, D, Romana, S, Radford-Weiss, I, Gross, F, Valensi, F, Delabesse, E