-
1
-
-
0031811713
-
A study to determine whether trisomy 8, deleted 9q and trisomy 22 are markers of cryptic rearrangements of PML/RAR a, AML1/ETO and CBFB/MYH11 respectively in acute myeloid leukemia
-
Langabeer S.E., Grimwade D., Walker H., Rogers J.R., Burnett A.K., Goldstone A.H., Linch D.C. A study to determine whether trisomy 8, deleted 9q and trisomy 22 are markers of cryptic rearrangements of PML/RAR a, AML1/ETO and CBFB/MYH11 respectively in acute myeloid leukemia. Br J Haematol. 101:1998;338-340.
-
(1998)
Br J Haematol
, vol.101
, pp. 338-340
-
-
Langabeer, S.E.1
Grimwade, D.2
Walker, H.3
Rogers, J.R.4
Burnett, A.K.5
Goldstone, A.H.6
Linch, D.C.7
-
2
-
-
0007759625
-
Impact of diagnostic cytogenetics on outcome in AML analysis of 1,613 patients entered into the UK MRC AML 10 trial
-
Grimwade D., Walker H., Harrison C., Oliver F., Wheatley K., Harrison G., Gray R., Hann I., Stevens R., Goldstone A., Burnett A. Impact of diagnostic cytogenetics on outcome in AML analysis of 1,613 patients entered into the UK MRC AML 10 trial. Blood. 88(Suppl 1):1996;2525a.
-
(1996)
Blood
, vol.88
, pp. 2525a
-
-
Grimwade, D.1
Walker, H.2
Harrison, C.3
Oliver, F.4
Wheatley, K.5
Harrison, G.6
Gray, R.7
Hann, I.8
Stevens, R.9
Goldstone, A.10
Burnett, A.11
-
3
-
-
0024458243
-
Is trisomy 22 in acute myeloid leukemia a primary abnormality or only a secondary change associated with inversion 16?
-
Grois N., Nowotony H., Tyl E., Krieger O., Kier P., Haas O.A. Is trisomy 22 in acute myeloid leukemia a primary abnormality or only a secondary change associated with inversion 16? Cancer Genet Cytogenet. 43:1989;119-129.
-
(1989)
Cancer Genet Cytogenet
, vol.43
, pp. 119-129
-
-
Grois, N.1
Nowotony, H.2
Tyl, E.3
Krieger, O.4
Kier, P.5
Haas, O.A.6
-
4
-
-
0028224763
-
Secondary chromosomal abnormalities in acute leukemias
-
Johansson B., Mertens F., Mitelman F. Secondary chromosomal abnormalities in acute leukemias. Leukemia. 8:1994;953-962.
-
(1994)
Leukemia
, vol.8
, pp. 953-962
-
-
Johansson, B.1
Mertens, F.2
Mitelman, F.3
-
5
-
-
20244365471
-
Detection of the chromosome 16 CBF β-MYH11 fusion transcript in myelomonocytic leukemias
-
Poirel H., Radford-Weiss I., Rack K., Troussard X., Veil A., Valensi F., Picard F., Guesnu M., Leboeuf D., Melle J., Dreyfus F., Flandrin G., Macintyre E. Detection of the chromosome 16 CBF β-MYH11 fusion transcript in myelomonocytic leukemias. Blood. 85:1995;1313-1322.
-
(1995)
Blood
, vol.85
, pp. 1313-1322
-
-
Poirel, H.1
Radford-Weiss, I.2
Rack, K.3
Troussard, X.4
Veil, A.5
Valensi, F.6
Picard, F.7
Guesnu, M.8
Leboeuf, D.9
Melle, J.10
Dreyfus, F.11
Flandrin, G.12
MacIntyre, E.13
-
6
-
-
0027373893
-
Fusion between transcription factor CBF-β/PEBP-2-β And a myosin heavy chain in acute myeloid leukemia
-
Liu P., Tarle S.A., Hajra A., Claton D.F., Marlton P., Freedman M., Siciliano M.J., Collins F.S. Fusion between transcription factor CBF-β/PEBP-2-β and a myosin heavy chain in acute myeloid leukemia. Science. 261:1993;1041-1044.
-
(1993)
Science
, vol.261
, pp. 1041-1044
-
-
Liu, P.1
Tarle, S.A.2
Hajra, A.3
Claton, D.F.4
Marlton, P.5
Freedman, M.6
Siciliano, M.J.7
Collins, F.S.8
-
7
-
-
0027519654
-
Identification of an inversion 16 coexisting with an isochromosome 22q by in situ hybridization in a case of childhood AML M4e
-
Gad S.G., Callen D.F., Kuss B., Dowing J.R., Behm F., Head D., Ribeiro R.C., Raimondi S.C. Identification of an inversion 16 coexisting with an isochromosome 22q by in situ hybridization in a case of childhood AML M4e. Leukemia. 7:1993;1658-1662.
-
(1993)
Leukemia
, vol.7
, pp. 1658-1662
-
-
Gad, S.G.1
Callen, D.F.2
Kuss, B.3
Dowing, J.R.4
Behm, F.5
Head, D.6
Ribeiro, R.C.7
Raimondi, S.C.8
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