-
1
-
-
34848904494
-
Myelodysplastic syndrome with isolated deletion of chromosome 20q: an indolent disease with minimal morphological dysplasia and frequent thrombocytopenic presentation
-
Gupta R., Soupir C.P., Johari V., et al. Myelodysplastic syndrome with isolated deletion of chromosome 20q: an indolent disease with minimal morphological dysplasia and frequent thrombocytopenic presentation. Br J Haematol 2007, 139:265-268.
-
(2007)
Br J Haematol
, vol.139
, pp. 265-268
-
-
Gupta, R.1
Soupir, C.P.2
Johari, V.3
-
2
-
-
25444484409
-
Identification of novel cytogenetic markers with prognostic significance in a series of 968 patients with primary myelodysplastic syndromes
-
Sole F., Luno E., Sanzo C., et al. Identification of novel cytogenetic markers with prognostic significance in a series of 968 patients with primary myelodysplastic syndromes. Haematologica 2005, 90:1168-1178.
-
(2005)
Haematologica
, vol.90
, pp. 1168-1178
-
-
Sole, F.1
Luno, E.2
Sanzo, C.3
-
3
-
-
0037353282
-
Clonal cytogenetic abnormalities in bone marrow specimens without clear morphologic evidence of dysplasia: a form fruste of myelodysplasia?
-
Steensma D.P., Dewald G.W., Hodnefield J.M., et al. Clonal cytogenetic abnormalities in bone marrow specimens without clear morphologic evidence of dysplasia: a form fruste of myelodysplasia?. Leuk Res 2003, 27:235-242.
-
(2003)
Leuk Res
, vol.27
, pp. 235-242
-
-
Steensma, D.P.1
Dewald, G.W.2
Hodnefield, J.M.3
-
4
-
-
79958726106
-
Characteristics and outcome of myelodysplastic syndromes (MDS) with isolated 20q deletion: a report on 62 cases
-
Braun T., de Botton S., Taksin A.L., et al. Characteristics and outcome of myelodysplastic syndromes (MDS) with isolated 20q deletion: a report on 62 cases. Leuk Res 2011, 35:863-867.
-
(2011)
Leuk Res
, vol.35
, pp. 863-867
-
-
Braun, T.1
de Botton, S.2
Taksin, A.L.3
-
5
-
-
48749090278
-
Therapy-related myeloid leukemia
-
Godley L.A., Larson R.A. Therapy-related myeloid leukemia. Semin Oncol 2008, 35:418-429.
-
(2008)
Semin Oncol
, vol.35
, pp. 418-429
-
-
Godley, L.A.1
Larson, R.A.2
-
6
-
-
0038305924
-
Clinical-cytogenetic associations in 306 patients with therapy-related myelodysplasia and myeloid leukemia: the University of Chicago series
-
Smith S.M., Le Beau M.M., Huo D., et al. Clinical-cytogenetic associations in 306 patients with therapy-related myelodysplasia and myeloid leukemia: the University of Chicago series. Blood 2003, 102:43-52.
-
(2003)
Blood
, vol.102
, pp. 43-52
-
-
Smith, S.M.1
Le Beau, M.M.2
Huo, D.3
-
7
-
-
53249123632
-
-
International Agency for Research on Cancer Press, Lyon, France, S.H. Swerdlow, E. Campo, N.L. Harris (Eds.)
-
WHO classification of tumours of haematopoietic and lymphoid tissues 2008, International Agency for Research on Cancer Press, Lyon, France. S.H. Swerdlow, E. Campo, N.L. Harris (Eds.).
-
(2008)
WHO classification of tumours of haematopoietic and lymphoid tissues
-
-
-
8
-
-
80054841733
-
Atypical cytogenetics in therapy-related myelodysplastic syndrome secondary to indolent B-cell lymphoma
-
Sinsabaugh C. Atypical cytogenetics in therapy-related myelodysplastic syndrome secondary to indolent B-cell lymphoma. Clin Lab Sci 2011, 24:142-146.
-
(2011)
Clin Lab Sci
, vol.24
, pp. 142-146
-
-
Sinsabaugh, C.1
-
9
-
-
0025741497
-
Therapy related myelodysplastic syndrome and leukemia with no " unfavourable" cytogenetic findings have a good response to intensive chemotherapy: a report on 15 cases
-
Fenaux P., Laï J.L., Quiquandon I., et al. therapy related myelodysplastic syndrome and leukemia with no " unfavourable" cytogenetic findings have a good response to intensive chemotherapy: a report on 15 cases. Leuk Lymphoma 1991, 5:117-125.
-
(1991)
Leuk Lymphoma
, vol.5
, pp. 117-125
-
-
Fenaux, P.1
Laï, J.L.2
Quiquandon, I.3
-
10
-
-
18744408734
-
Mantle cell lymphoma with 8q24 chromosomal abnormalities: a report of 5 cases with blastoid features
-
Hao S., Sanger W., Onciu M., et al. Mantle cell lymphoma with 8q24 chromosomal abnormalities: a report of 5 cases with blastoid features. Mod Pathol 2002, 15:1266-1272.
-
(2002)
Mod Pathol
, vol.15
, pp. 1266-1272
-
-
Hao, S.1
Sanger, W.2
Onciu, M.3
-
12
-
-
79954432996
-
Chromosome 20q deletion: a recurrent cytogenetic abnormality in patients with chronic myelogenous leukemia in remission
-
Sun J., Yin C.C., Cui W., et al. Chromosome 20q deletion: a recurrent cytogenetic abnormality in patients with chronic myelogenous leukemia in remission. Am J Clin Pathol 2011, 135:391-397.
-
(2011)
Am J Clin Pathol
, vol.135
, pp. 391-397
-
-
Sun, J.1
Yin, C.C.2
Cui, W.3
-
13
-
-
0030897009
-
International scoring system for evaluating prognosis in myelodysplastic syndromes
-
Greenberg P., Cox C., LeBeau M.M., et al. International scoring system for evaluating prognosis in myelodysplastic syndromes. Blood 1997, 89:2079-2088.
-
(1997)
Blood
, vol.89
, pp. 2079-2088
-
-
Greenberg, P.1
Cox, C.2
LeBeau, M.M.3
-
14
-
-
0742324488
-
Karyotype is an independent prognostic parameter in therapy-related acute myeloid leukemia (t-AML): an analysis of 93 patients with t-AML in comparison to 1091 patients with de novo AML
-
Schoch C., Kern W., Schnittger S., et al. Karyotype is an independent prognostic parameter in therapy-related acute myeloid leukemia (t-AML): an analysis of 93 patients with t-AML in comparison to 1091 patients with de novo AML. Leukemia 2003, 18:120-125.
-
(2003)
Leukemia
, vol.18
, pp. 120-125
-
-
Schoch, C.1
Kern, W.2
Schnittger, S.3
-
15
-
-
39649094569
-
New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: evidence from a core dataset of 2124 patients
-
Haase D., Germing U., Schanz J., et al. New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: evidence from a core dataset of 2124 patients. Blood 2007, 110:4385-4395.
-
(2007)
Blood
, vol.110
, pp. 4385-4395
-
-
Haase, D.1
Germing, U.2
Schanz, J.3
-
16
-
-
84858830672
-
New comprehensive cytogenetic scoring system for primary myelodysplastic syndromes (MDS) and oligoblastic acute myeloid leukemia after MDS derived from an international database merge
-
Schanz J., Tuchler H., Sole F., et al. New comprehensive cytogenetic scoring system for primary myelodysplastic syndromes (MDS) and oligoblastic acute myeloid leukemia after MDS derived from an international database merge. J Clin Oncol 2012, 30:820-829.
-
(2012)
J Clin Oncol
, vol.30
, pp. 820-829
-
-
Schanz, J.1
Tuchler, H.2
Sole, F.3
-
17
-
-
84857363893
-
Morphology, cytogenetics, and survival in myelodysplasia with del(20q) or ider(20q): a multicenter study
-
Mullier F., Daliphard S., Garand R., et al. Morphology, cytogenetics, and survival in myelodysplasia with del(20q) or ider(20q): a multicenter study. Ann Hematol 2012, 91:203-213.
-
(2012)
Ann Hematol
, vol.91
, pp. 203-213
-
-
Mullier, F.1
Daliphard, S.2
Garand, R.3
-
18
-
-
77949372605
-
Characterization of chromosome arm 20q abnormalities in myeloid malignancies using genome-wide single nucleotide polymorphism array analysis
-
Huh J., Tiu R.V., Gondek L.P., et al. Characterization of chromosome arm 20q abnormalities in myeloid malignancies using genome-wide single nucleotide polymorphism array analysis. Genes Chromosomes Cancer 2010, 49:390-399.
-
(2010)
Genes Chromosomes Cancer
, vol.49
, pp. 390-399
-
-
Huh, J.1
Tiu, R.V.2
Gondek, L.P.3
-
19
-
-
0029846342
-
Hematologic disorders associated with deletions of chromosome 20q: a clinicopathologic study of 107 patients
-
Kurtin P.J., Dewald G.W., Shields D.J., et al. Hematologic disorders associated with deletions of chromosome 20q: a clinicopathologic study of 107 patients. Am J Clin Pathol 1996, 106:680-688.
-
(1996)
Am J Clin Pathol
, vol.106
, pp. 680-688
-
-
Kurtin, P.J.1
Dewald, G.W.2
Shields, D.J.3
-
20
-
-
33947101019
-
Patterns of somatic mutation in human cancer genomes
-
Greenman C., Stephens P., Smith R., et al. Patterns of somatic mutation in human cancer genomes. Nature 2007, 446:153-158.
-
(2007)
Nature
, vol.446
, pp. 153-158
-
-
Greenman, C.1
Stephens, P.2
Smith, R.3
-
21
-
-
79959811310
-
Applications of fluorescence in situ hybridization (FISH) in detecting genetic aberrations of medical significance
-
Bishop R. Applications of fluorescence in situ hybridization (FISH) in detecting genetic aberrations of medical significance. Bioscience Horizons 2010, 3:85-95.
-
(2010)
Bioscience Horizons
, vol.3
, pp. 85-95
-
-
Bishop, R.1
|