AAAAAA

   
Results: 1-4 |
Results: 4

Authors: Menasche, G Pastural, E Feldmann, J Certain, S Ersoy, F Dupuis, S Wulffraat, N Bianchi, D Fischer, A Le Deist, F de Saint Basile, G
Citation: G. Menasche et al., Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome, NAT GENET, 25(2), 2000, pp. 173-176

Authors: Cavazzana-Calvo, M Hacein-Bey, S Basile, CD Gross, F Yvon, E Nusbaum, P Selz, F Hue, C Certain, S Casanova, JL Bousso, P Le Deist, F Fischer, A
Citation: M. Cavazzana-calvo et al., Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease, SCIENCE, 288(5466), 2000, pp. 669-672

Authors: Certain, S Barrat, F Pastural, E Le Deist, F Goyo-Rivas, J Jabado, N Benkerrou, M Seger, R Vilmer, E Beullier, G Schwarz, K Fischer, A de Saint Basile, G
Citation: S. Certain et al., Protein truncation test of LYST reveals heterogenous mutations in patientswith Chediak-Higashi syndrome, BLOOD, 95(3), 2000, pp. 979-983

Authors: Stepp, SE Dufourcq-Lagelouse, R Le Deist, F Bhawan, S Certain, S Mathew, PA Henter, JI Bennett, M Fischer, A Saint Basile, GD Kumar, V
Citation: Se. Stepp et al., Perforin gene defects in familiar hemophagocytic lymphohistiocytosis, SCIENCE, 286(5446), 1999, pp. 1957-1959
Risultati: 1-4 |