3 results for author:"Pages M.-P." in Literature citations
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| Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions. Quentin S., Cuccuini W., Ceccaldi R., Nibourel O., Pondarre C., Pages M.P., Vasquez N., Dubois d'Enghien C., Larghero J., Peffault de Latour R. et al. Blood 117:e161-70(2011) · Mapped (2) |
| Wide diversity of PAX5 alterations in B-ALL: a Groupe Francophone de Cytogenetique Hematologique study. Coyaud E., Struski S., Prade N., Familiades J., Eichner R., Quelen C., Bousquet M., Mugneret F., Talmant P., Pages M.P. et al. Blood 115:3089-3097(2010) · Mapped (21) |
| Clinical significance of HOX11L2 expression linked to t(5;14)(q35;q32), of HOX11 expression, and of SIL-TAL fusion in childhood T-cell malignancies: results of EORTC studies 58881 and 58951. Cave H., Suciu S., Preudhomme C., Poppe B., Robert A., Uyttebroeck A., Malet M., Boutard P., Benoit Y., Mauvieux L. et al. |