M. Busson‐Le Coniat

Recurrence of OTT–MAL fusion in t(1;22) of infant AML‐M7

R. Berger, O. Bernard, N. Dastugue, 2002, Genes, chromosomes & cancer.

The t(1;12)(q21;p13) translocation of human acute myeloblastic leukemia results in a TEL-ARNT fusion.

R. Berger, O. Bernard, J. Ghysdael, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Chromosome studies of in vitro senescent lymphocytes: nonrandom trisomy 2.

G. Thomas, H. Blanché, R. Berger, 2002, Annales de genetique.

Transcriptional analysis of the orphan nuclear receptor constitutive androstane receptor (NR1I3) gene promoter: identification of a distal glucocorticoid response element.

J. Pascussi, P. Maurel, M. Busson‐Le Coniat, 2003, Molecular endocrinology.

Acute megakaryocytic leukaemia with acquired polysomy 21 and translocation t(1;21).

R. Berger, M. Busson‐Le Coniat, S. Paulien, 2000, Annales de genetique.

HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis.

J. Zucman‐Rossi, R. Berger, O. Bernard, 2002, Blood.

Chromosome 21 abnormalities with AML1 amplification in acute lymphoblastic leukemia

R. Berger, O. Bernard, M. Daniel, 2001, Genes, chromosomes & cancer.

Complex chromosome abnormality mimicking t(8;21)in an acute myeloblastic leukemia.

R. Berger, M. Daniel, M. Busson‐Le Coniat, 2001, Annales de Genetique.