-
1
-
-
33746470443
-
A t(17;20)(q21;q12) masking a variant t(15;17)(q22;q21) in a patient with acute promyelocytic leukemia
-
Garcia-Casado Z., Cervera J., Valencia A., Pajuelo J.C., Mena-Duran A.V., Barragan E., Bolufer P., and Sanz M.A. A t(17;20)(q21;q12) masking a variant t(15;17)(q22;q21) in a patient with acute promyelocytic leukemia. Cancer Genet Cytogenet 168 (2006) 73-76
-
(2006)
Cancer Genet Cytogenet
, vol.168
, pp. 73-76
-
-
Garcia-Casado, Z.1
Cervera, J.2
Valencia, A.3
Pajuelo, J.C.4
Mena-Duran, A.V.5
Barragan, E.6
Bolufer, P.7
Sanz, M.A.8
-
2
-
-
0032900687
-
Complex variant 15;17 translocations in acute promyelocytic leukemia: a case report and review of three-way translocations
-
Wan T.S., Chim C.S., So C.K., Chan L.C., and Ma S.K. Complex variant 15;17 translocations in acute promyelocytic leukemia: a case report and review of three-way translocations. Cancer Genet Cytogenet 111 (1999) 139-143
-
(1999)
Cancer Genet Cytogenet
, vol.111
, pp. 139-143
-
-
Wan, T.S.1
Chim, C.S.2
So, C.K.3
Chan, L.C.4
Ma, S.K.5
-
3
-
-
33746199926
-
A complex, four-way variant t(15;17) in acute promyelocytic leukemia
-
Yoo S.J., Seo E.J., Lee J.H., Seo Y.H., Park P.W., and Ahn J.Y. A complex, four-way variant t(15;17) in acute promyelocytic leukemia. Cancer Genet Cytogenet 167 (2006) 168-171
-
(2006)
Cancer Genet Cytogenet
, vol.167
, pp. 168-171
-
-
Yoo, S.J.1
Seo, E.J.2
Lee, J.H.3
Seo, Y.H.4
Park, P.W.5
Ahn, J.Y.6
-
4
-
-
0032053375
-
A new variant translocation of t(15;17) in a patient with acute promyelocytic leukemia (M3): t(15;19;17)(q22;p13;q12)
-
Saitoh K., Miura I., Kobayashi Y., Kume M., Utsumi S., Takahashi N., Hatano Y., Nimura T., Hashimoto K., Takahashi S., and Miura A.B. A new variant translocation of t(15;17) in a patient with acute promyelocytic leukemia (M3): t(15;19;17)(q22;p13;q12). Cancer Genet Cytogenet 102 (1998) 15-18
-
(1998)
Cancer Genet Cytogenet
, vol.102
, pp. 15-18
-
-
Saitoh, K.1
Miura, I.2
Kobayashi, Y.3
Kume, M.4
Utsumi, S.5
Takahashi, N.6
Hatano, Y.7
Nimura, T.8
Hashimoto, K.9
Takahashi, S.10
Miura, A.B.11
-
5
-
-
23244447162
-
Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion
-
Tirado C.A., Jahn J.A., Scheerle J., Eid M., Meister R.J., Christie R.J., Croft C.D., Wallingford S., Heritage D.W., Mowrey P.N., and Meloni-Ehrig A.M. Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion. Cancer Genet Cytogenet 161 (2005) 70-73
-
(2005)
Cancer Genet Cytogenet
, vol.161
, pp. 70-73
-
-
Tirado, C.A.1
Jahn, J.A.2
Scheerle, J.3
Eid, M.4
Meister, R.J.5
Christie, R.J.6
Croft, C.D.7
Wallingford, S.8
Heritage, D.W.9
Mowrey, P.N.10
Meloni-Ehrig, A.M.11
-
6
-
-
0002789260
-
Classical and molecular cytogenetics of tumor cells
-
Wegner R.D. (Ed), Springer, Berlin
-
Schlegelberger B., Metzke S., Harder S., Zühlke-Jenisch R., Zhang Y., and Siebert R. Classical and molecular cytogenetics of tumor cells. In: Wegner R.D. (Ed). Diagnostic cytogenetics (1999), Springer, Berlin 151-185
-
(1999)
Diagnostic cytogenetics
, pp. 151-185
-
-
Schlegelberger, B.1
Metzke, S.2
Harder, S.3
Zühlke-Jenisch, R.4
Zhang, Y.5
Siebert, R.6
-
7
-
-
34247898410
-
-
ISCN 1995: an international system for human cytogenetic nomenclature (1995). Mitelman F, editor. Basel: S. Karger, 1995.
-
-
-
-
8
-
-
24744463904
-
Standardised fluorescence in situ hybridisation in cytological and histological specimens
-
Wilkens L., Gerr H., Gadzicki D., Kreipe H., and Schlegelberger B. Standardised fluorescence in situ hybridisation in cytological and histological specimens. Virchows Arch 447 (2005) 586-592
-
(2005)
Virchows Arch
, vol.447
, pp. 586-592
-
-
Wilkens, L.1
Gerr, H.2
Gadzicki, D.3
Kreipe, H.4
Schlegelberger, B.5
-
9
-
-
7844223626
-
Detection of karyotypic aberrations in acute myeloblastic leukaemia: a prospective comparison between PCR/FISH and standard cytogenetics in 140 patients with de novo AML
-
Krauter J., Peter W., Pascheberg U., Heinze B., Bergmann L., Hoelzer D., Lubbert M., Schlimok G., Arnold R., Kirchner H., Port M., Ganser A., and Heil G. Detection of karyotypic aberrations in acute myeloblastic leukaemia: a prospective comparison between PCR/FISH and standard cytogenetics in 140 patients with de novo AML. Br J Haematol 103 (1998) 72-78
-
(1998)
Br J Haematol
, vol.103
, pp. 72-78
-
-
Krauter, J.1
Peter, W.2
Pascheberg, U.3
Heinze, B.4
Bergmann, L.5
Hoelzer, D.6
Lubbert, M.7
Schlimok, G.8
Arnold, R.9
Kirchner, H.10
Port, M.11
Ganser, A.12
Heil, G.13
-
10
-
-
0034494569
-
Additional chromosomal abnormalities in patients with acute promyelocytic leukaemia (APL) do not confer poor prognosis: results of APL 93 trial
-
European APL Group
-
de Botton S., Chevret S., Sanz M., Dombret H., Thomas X., Guerci A., Fey M., Rayon C., Huguet F., Sotto J.J., Gardin C., Cony Makhoul P., Travade P., Solary E., Fegueux N., Bordessoule D., San Miguel J., Link H., Desablens B., Stamatoullas A., Deconinck E., Geiser K., Hess U., Maloisel F., Castaigne S., Preudhomme C., Chomienne C., Degos L., Fenaux P., and European APL Group. Additional chromosomal abnormalities in patients with acute promyelocytic leukaemia (APL) do not confer poor prognosis: results of APL 93 trial. Br J Haematol 111 (2000) 801-806
-
(2000)
Br J Haematol
, vol.111
, pp. 801-806
-
-
de Botton, S.1
Chevret, S.2
Sanz, M.3
Dombret, H.4
Thomas, X.5
Guerci, A.6
Fey, M.7
Rayon, C.8
Huguet, F.9
Sotto, J.J.10
Gardin, C.11
Cony Makhoul, P.12
Travade, P.13
Solary, E.14
Fegueux, N.15
Bordessoule, D.16
San Miguel, J.17
Link, H.18
Desablens, B.19
Stamatoullas, A.20
Deconinck, E.21
Geiser, K.22
Hess, U.23
Maloisel, F.24
Castaigne, S.25
Preudhomme, C.26
Chomienne, C.27
Degos, L.28
Fenaux, P.29
more..
-
11
-
-
0031040058
-
Additional chromosome abnormalities confer worse prognosis in acute promyelocytic leukaemia
-
Hiorns L.R., Swansbury G.J., Mehta J., Min T., Dainton M.G., Treleaven J., Powles R.L., and Catovsky D. Additional chromosome abnormalities confer worse prognosis in acute promyelocytic leukaemia. Br J Haematol 96 (1997) 314-321
-
(1997)
Br J Haematol
, vol.96
, pp. 314-321
-
-
Hiorns, L.R.1
Swansbury, G.J.2
Mehta, J.3
Min, T.4
Dainton, M.G.5
Treleaven, J.6
Powles, R.L.7
Catovsky, D.8
-
12
-
-
0030912485
-
Secondary cytogenetic changes in acute promyelocytic leukemia: prognostic importance in patients treated with chemotherapy alone and association with the intron 3 breakpoint of the PML gene: a Cancer and Leukemia Group B study
-
Slack J.L., Arthur D.C., Lawrence D., Mrozek K., Mayer R.J., Davey F.R., Tantravahi R., Pettenati M.J., Bigner S., Carroll A.J., Rao K.W., Schiffer C.A., and Bloomfield C.D. Secondary cytogenetic changes in acute promyelocytic leukemia: prognostic importance in patients treated with chemotherapy alone and association with the intron 3 breakpoint of the PML gene: a Cancer and Leukemia Group B study. J Clin Oncol 15 (1997) 1786-1795
-
(1997)
J Clin Oncol
, vol.15
, pp. 1786-1795
-
-
Slack, J.L.1
Arthur, D.C.2
Lawrence, D.3
Mrozek, K.4
Mayer, R.J.5
Davey, F.R.6
Tantravahi, R.7
Pettenati, M.J.8
Bigner, S.9
Carroll, A.J.10
Rao, K.W.11
Schiffer, C.A.12
Bloomfield, C.D.13
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