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leukemia chromosome ds-all syndrome lymphoblastic leukemia etv 6 cytogenetic ds-aml study blood cancer translocation hlxb 9 patient children lymphoblastic abnormality fusion table number myeloid aberration chromosomal figure change cancer genet cytogenet genes chromosomes cancer c 7orf erasmus mc myeloid leukemia breakpoint feature anomaly signi ficantly signi transcript megakaryoblastic leukemia leukaemia rearrangement ͻ.001 childhood forestier protein frequency imbalance chromosomal abnormalities 7 q 36 genet chromosomal aberrations ficantly cytogenetically series erasmu pattern university homeobox primers johansson b department cytogenet karyotypic 2011. 9-etv analyses megakaryoblastic group library sequence myeloid leukemias cytogenetic features volume gata 1 mutations hyperdiploidy february syndrome blood american society partner b-cell precursor johansson ds-amkl
2 Most Recent Publications
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Cytogenetic features of acute lymphoblastic and myeloid leukemias in pediatric patients with Down syndrome: An iBFM-SG study
(Article)
Forestier, E. Izraeli, S. Beverloo, H.B. Haas, O.A. Pession, A. Michalová, K. Stark, B. Harrison, C.J. Teigler-Schlegel, A. Johansson, B. |
2008-02-12
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Fusion of the homeobox gene HLXB9 and the ETV6 gene in infant acute myeloid leukemias with the t(7;12)(q36;p13)
(Article)
Beverloo, H.B. Panagopoulos, I. Isaksson, M. Wering, E.R. van Drunen, E. van Klein, J.E.M.M. de Johansson, B. Slater, R. |
2001-01-01
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