Authors:
Elghezal, H
Le Guyader, G
Radford-Weiss, I
Perot, C
Van den Akker, J
Eydoux, P
Vekemans, M
Romana, SP
Citation: H. Elghezal et al., Reassessment of childhood B-Lineage lymphoblastic leukemia karyotypes using spectral analysis, GENE CHROM, 30(4), 2001, pp. 383-392
Authors:
Megarbane, B
Bodemer, C
Valensi, F
Radford-Weiss, I
Fraitag, S
MacIntyre, E
Bletry, O
Varet, B
Hermine, O
Citation: B. Megarbane et al., Association of acute neutrophilic dermatosis and myelodysplastic syndrome with (6;9) chromosome translocation: a case report and review of the literature, BR J DERM, 143(6), 2000, pp. 1322-1324
Authors:
Grimwade, D
Biondi, A
Mozziconacci, MJ
Hagemeijer, A
Berger, R
Neat, M
Howe, K
Dastugue, N
Jansen, J
Radford-Weiss, I
Lo Coco, F
Lessard, M
Hernandez, JM
Delabesse, E
Head, D
Liso, V
Sainty, D
Flandrin, G
Solomon, E
Birg, F
Lafage-Pochitaloff, M
Citation: D. Grimwade et al., Characterization of acute promyelocytic leukemia cases lacking the classict(15;17): results of the European Working Party, BLOOD, 96(4), 2000, pp. 1297-1308
Authors:
Emile, JF
Geissmann, F
Martin, OD
Radford-Weiss, I
Lepelletier, Y
Heymer, B
Espanol, T
de Santes, KB
Bertrand, Y
Brousse, N
Casanova, JL
Fischer, A
Citation: Jf. Emile et al., Langerhans cell deficiency in reticular dysgenesis, BLOOD, 96(1), 2000, pp. 58-62
Authors:
Harrison, CJ
Radford-Weiss, I
Ross, F
Rack, K
le Guyader, G
Vekemans, M
Macintyre, E
Citation: Cj. Harrison et al., Fluorescence in situ hybridization analysis of masked (8;21)(q22;q22) translocations, CANC GENET, 112(1), 1999, pp. 15-20
Authors:
Mauvieux, L
Delabesse, E
Bourquelot, P
Radford-Weiss, I
Bennaceur, AL
Flandrin, G
Valensi, F
Macintyre, EA
Citation: L. Mauvieux et al., NG2 expression in MLL rearranged acute myeloid leukaemia is restricted to monoblastic cases, BR J HAEM, 107(3), 1999, pp. 674-676