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Page 1
Acute megakaryoblastic leukemia and loss of the RUNX1 gene.
Berger R, Busson M, Dastugue N, Radford-Weiss I, Michaux L, Hagemeijer A, Quilichini B, Benattar L, Bernard O, Romana SP. Berger R, et al. Among authors: busson m. Cancer Genet Cytogenet. 2006 Jan 1;164(1):71-3. doi: 10.1016/j.cancergencyto.2005.05.002. Cancer Genet Cytogenet. 2006. PMID: 16364766
Identical abnormality of the short arm of chromosome 18 in two Philadelphia-positive chronic myelocytic leukemia patients with erythroblastic transformation, resulting in duplication of BCR-ABL1 fusion.
Nguyen Khac F, Waill MC, Romana SP, Radford-Weiss I, Busson M, Collonge-Rame MA, Ribadeau-Dumas A, Piffaut MC, Daniel MT, Davi F, Merle-Béral H, Berger R, Arock M. Nguyen Khac F, et al. Among authors: busson m. Cancer Genet Cytogenet. 2002 Oct 1;138(1):22-6. doi: 10.1016/s0165-4608(02)00574-5. Cancer Genet Cytogenet. 2002. PMID: 12419580
t(5;14)/HOX11L2-positive T-cell acute lymphoblastic leukemia. A collaborative study of the Groupe Français de Cytogénétique Hématologique (GFCH).
Berger R, Dastugue N, Busson M, Van Den Akker J, Pérot C, Ballerini P, Hagemeijer A, Michaux L, Charrin C, Pages MP, Mugneret F, Andrieux J, Talmant P, Hélias C, Mauvieux L, Lafage-Pochitaloff M, Mozziconacci MJ, Cornillet-Lefebvre P, Radford I, Asnafi V, Bilhou-Nabera C, Nguyen Khac F, Léonard C, Speleman F, Poppe B, Bastard C, Taviaux S, Quilichini B, Herens C, Grégoire MJ, Cavé H, Bernard OA; Groupe Français de Cytogénétique Hématologique (GFCH). Berger R, et al. Among authors: busson m. Leukemia. 2003 Sep;17(9):1851-7. doi: 10.1038/sj.leu.2403061. Leukemia. 2003. PMID: 12970786
214 results