-
1
-
-
66249137734
-
Mutation in TET2 in myeloid cancers
-
Delhommeau F, Dupont S, Della Valle V, et al. Mutation in TET2 in myeloid cancers. N Engl J Med. 2009;360(22):2289-2301.
-
(2009)
N Engl J Med
, vol.360
, Issue.22
, pp. 2289-2301
-
-
Delhommeau, F.1
Dupont, S.2
Della Valle, V.3
-
2
-
-
66849124925
-
Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia
-
Gelsi-Boyer V, Trouplin V, Adéläide J, et al. Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia. Br J Haematol. 2009; 145(6):788-800.
-
(2009)
Br J Haematol
, vol.145
, Issue.6
, pp. 788-800
-
-
Gelsi-Boyer, V.1
Trouplin, V.2
Adéläide, J.3
-
3
-
-
84885021313
-
Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms
-
Kon A, Shih LY, Minamino M, et al. Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms. Nat Genet. 2013; 45(10):1232-1237.
-
(2013)
Nat Genet
, vol.45
, Issue.10
, pp. 1232-1237
-
-
Kon, A.1
Shih, L.Y.2
Minamino, M.3
-
4
-
-
80054010617
-
Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts
-
Papaemmanuil E, Cazzola M, Boultwood J, et al; Chronic Myeloid Disorders Working Group of the International Cancer Genome Consortium. Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts. N Engl J Med. 2011;365(15): 1384-1395.
-
(2011)
N Engl J Med
, vol.365
, Issue.15
, pp. 1384-1395
-
-
Papaemmanuil, E.1
Cazzola, M.2
Boultwood, J.3
-
5
-
-
80053900941
-
Frequent pathway mutations of splicing machinery in myelodysplasia
-
Yoshida K, Sanada M, Shiraishi Y, et al. Frequent pathway mutations of splicing machinery in myelodysplasia. Nature. 2011;478(7367):64-69.
-
(2011)
Nature
, vol.478
, Issue.7367
, pp. 64-69
-
-
Yoshida, K.1
Sanada, M.2
Shiraishi, Y.3
-
6
-
-
84893772765
-
Landscape of genetic lesions in 944 patients with myelodysplastic syndromes
-
Haferlach T, Nagata Y, Grossmann V, et al. Landscape of genetic lesions in 944 patients with myelodysplastic syndromes. Leukemia. 2014; 28(2):241-247.
-
(2014)
Leukemia
, vol.28
, Issue.2
, pp. 241-247
-
-
Haferlach, T.1
Nagata, Y.2
Grossmann, V.3
-
7
-
-
84888219405
-
Clinical and biological implications of driver mutations in myelodysplastic syndromes
-
quiz 3699
-
Papaemmanuil E, Gerstung M, Malcovati L, et al; Chronic Myeloid Disorders Working Group of the International Cancer Genome Consortium. Clinical and biological implications of driver mutations in myelodysplastic syndromes. Blood. 2013;122(22):3616-3627, quiz 3699.
-
(2013)
Blood
, vol.122
, Issue.22
, pp. 3616-3627
-
-
Papaemmanuil, E.1
Gerstung, M.2
Malcovati, L.3
-
8
-
-
84961554506
-
Acute myeloid leukemia ontogeny is defined by distinct somatic mutations
-
Lindsley RC, Mar BG, Mazzola E, et al. Acute myeloid leukemia ontogeny is defined by distinct somatic mutations. Blood. 2015;125(9): 1367-1376.
-
(2015)
Blood
, vol.125
, Issue.9
, pp. 1367-1376
-
-
Lindsley, R.C.1
Mar, B.G.2
Mazzola, E.3
-
9
-
-
77955085750
-
Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders
-
Ernst T, Chase AJ, Score J, et al. Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders. Nat Genet. 2010; 42(8):722-726.
-
(2010)
Nat Genet
, vol.42
, Issue.8
, pp. 722-726
-
-
Ernst, T.1
Chase, A.J.2
Score, J.3
-
10
-
-
65349193344
-
Skewing of X-inactivation ratios in blood cells of aging women is confirmed by independent methodologies
-
Busque L, Paquette Y, Provost S, et al. Skewing of X-inactivation ratios in blood cells of aging women is confirmed by independent methodologies. Blood. 2009;113(15):3472-3474.
-
(2009)
Blood
, vol.113
, Issue.15
, pp. 3472-3474
-
-
Busque, L.1
Paquette, Y.2
Provost, S.3
-
11
-
-
84873038844
-
Skewed X-inactivation patterns in ageing healthy and myelodysplastic haematopoiesis determined by a pyrosequencing based transcriptional clonality assay
-
Mossner M, Nolte F, Hütter G, et al. Skewed X-inactivation patterns in ageing healthy and myelodysplastic haematopoiesis determined by a pyrosequencing based transcriptional clonality assay. J Med Genet. 2013;50(2):108-117.
-
(2013)
J Med Genet
, vol.50
, Issue.2
, pp. 108-117
-
-
Mossner, M.1
Nolte, F.2
Hütter, G.3
-
12
-
-
84920024296
-
Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence
-
Genovese G, Kähler AK, Handsaker RE, et al. Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence. N Engl J Med. 2014;371(26):2477-2487.
-
(2014)
N Engl J Med
, vol.371
, Issue.26
, pp. 2477-2487
-
-
Genovese, G.1
Kähler, A.K.2
Handsaker, R.E.3
-
13
-
-
84920053873
-
Agerelated clonal hematopoiesis associated with adverse outcomes
-
Jaiswal S, Fontanillas P, Flannick J, et al. Agerelated clonal hematopoiesis associated with adverse outcomes. N Engl J Med. 2014;371(26): 2488-2498.
-
(2014)
N Engl J Med
, vol.371
, Issue.26
, pp. 2488-2498
-
-
Jaiswal, S.1
Fontanillas, P.2
Flannick, J.3
-
14
-
-
84930003179
-
Age-related mutations associated with clonal hematopoietic expansion and malignancies
-
Xie M, Lu C, Wang J, et al. Age-related mutations associated with clonal hematopoietic expansion and malignancies. Nat Med. 2014;20(12): 1472-1478.
-
(2014)
Nat Med
, vol.20
, Issue.12
, pp. 1472-1478
-
-
Xie, M.1
Lu, C.2
Wang, J.3
-
15
-
-
84868208186
-
Recurrent somatic TET2 mutations in normal elderly individuals with clonal hematopoiesis
-
Busque L, Patel JP, Figueroa ME, et al. Recurrent somatic TET2 mutations in normal elderly individuals with clonal hematopoiesis. Nat Genet. 2012;44(11):1179-1181.
-
(2012)
Nat Genet
, vol.44
, Issue.11
, pp. 1179-1181
-
-
Busque, L.1
Patel, J.P.2
Figueroa, M.E.3
-
16
-
-
84861628224
-
Detectable clonal mosaicism and its relationship to aging and cancer
-
Jacobs KB, Yeager M, Zhou W, et al. Detectable clonal mosaicism and its relationship to aging and cancer. Nat Genet. 2012;44(6):651-658.
-
(2012)
Nat Genet
, vol.44
, Issue.6
, pp. 651-658
-
-
Jacobs, K.B.1
Yeager, M.2
Zhou, W.3
-
17
-
-
84861591789
-
Detectable clonal mosaicism from birth to old age and its relationship to cancer
-
Laurie CC, Laurie CA, Rice K, et al. Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nat Genet. 2012;44(6): 642-650.
-
(2012)
Nat Genet
, vol.44
, Issue.6
, pp. 642-650
-
-
Laurie, C.C.1
Laurie, C.A.2
Rice, K.3
-
18
-
-
84987646661
-
Application of a short tandem repeat based PCR assay for chronological monitoring of myelodysplastic syndrome (MDS) patients with deletion of chromosome 5q following lenalidomide treatment [abstract]
-
Abstract 2891
-
Jann JC, Nowak D, Nolte F, et al. Application of a short tandem repeat based PCR assay for chronological monitoring of myelodysplastic syndrome (MDS) patients with deletion of chromosome 5q following lenalidomide treatment [abstract]. Blood. 2015;126(23). Abstract 2891.
-
(2015)
Blood
, vol.126
, Issue.23
-
-
Jann, J.C.1
Nowak, D.2
Nolte, F.3
-
19
-
-
84902200836
-
Myelodysplastic cells in patients reprogram mesenchymal stromal cells to establish a transplantable stem cell niche disease unit
-
Medyouf H, Mossner M, Jann JC, et al. Myelodysplastic cells in patients reprogram mesenchymal stromal cells to establish a transplantable stem cell niche disease unit. Cell Stem Cell. 2014;14(6):824-837.
-
(2014)
Cell Stem Cell
, vol.14
, Issue.6
, pp. 824-837
-
-
Medyouf, H.1
Mossner, M.2
Jann, J.C.3
-
20
-
-
77952568128
-
Engraftment of human hematopoietic stem cells is more efficient in female NOD/SCID/IL-2Rgc-null recipients
-
Notta F, Doulatov S, Dick JE. Engraftment of human hematopoietic stem cells is more efficient in female NOD/SCID/IL-2Rgc-null recipients. Blood. 2010;115(18):3704-3707.
-
(2010)
Blood
, vol.115
, Issue.18
, pp. 3704-3707
-
-
Notta, F.1
Doulatov, S.2
Dick, J.E.3
-
21
-
-
84952310964
-
SciClone: Inferring clonal architecture and tracking the spatial and temporal patterns of tumor evolution
-
Miller CA, White BS, Dees ND, et al. SciClone: inferring clonal architecture and tracking the spatial and temporal patterns of tumor evolution. PLOS Comput Biol. 2014;10(8):e1003665.
-
(2014)
PLOS Comput Biol
, vol.10
, Issue.8
-
-
Miller, C.A.1
White, B.S.2
Dees, N.D.3
-
22
-
-
84884996623
-
The integrated landscape of driver genomic alterations in glioblastoma
-
Frattini V, Trifonov V, Chan JM, et al. The integrated landscape of driver genomic alterations in glioblastoma. Nat Genet. 2013;45(10): 1141-1149.
-
(2013)
Nat Genet
, vol.45
, Issue.10
, pp. 1141-1149
-
-
Frattini, V.1
Trifonov, V.2
Chan, J.M.3
-
23
-
-
84894304555
-
Preleukemic mutations in human acute myeloid leukemia affect epigenetic regulators and persist in remission
-
Corces-Zimmerman MR, Hong WJ, Weissman IL, Medeiros BC, Majeti R. Preleukemic mutations in human acute myeloid leukemia affect epigenetic regulators and persist in remission. Proc Natl Acad Sci USA. 2014;111(7):2548-2553.
-
(2014)
Proc Natl Acad Sci USA
, vol.111
, Issue.7
, pp. 2548-2553
-
-
Corces-Zimmerman, M.R.1
Hong, W.J.2
Weissman, I.L.3
Medeiros, B.C.4
Majeti, R.5
-
24
-
-
84865827060
-
Clonal evolution of preleukemic hematopoietic stem cells precedes human acute myeloid leukemia
-
Jan M, Snyder TM, Corces-Zimmerman MR, et al. Clonal evolution of preleukemic hematopoietic stem cells precedes human acute myeloid leukemia. Sci Transl Med. 2012;4(149):149ra118.
-
(2012)
Sci Transl Med
, vol.4
, Issue.149
, pp. 149ra118
-
-
Jan, M.1
Snyder, T.M.2
Corces-Zimmerman, M.R.3
-
25
-
-
84916229685
-
Persistence of DNMT3A mutations at long-term remission in adult patients with AML
-
Pløen GG, Nederby L, Guldberg P, et al. Persistence of DNMT3A mutations at long-term remission in adult patients with AML. Br J Haematol. 2014;167(4):478-486.
-
(2014)
Br J Haematol
, vol.167
, Issue.4
, pp. 478-486
-
-
Pløen, G.G.1
Nederby, L.2
Guldberg, P.3
-
26
-
-
84894245627
-
Identification of pre-leukaemic haematopoietic stem cells in acute leukaemia
-
Shlush LI, Zandi S, Mitchell A, et al; HALT Pan- Leukemia Gene Panel Consortium. Identification of pre-leukaemic haematopoietic stem cells in acute leukaemia. Nature. 2014; 506(7488):328-333.
-
(2014)
Nature
, vol.506
, Issue.7488
, pp. 328-333
-
-
Shlush, L.I.1
Zandi, S.2
Mitchell, A.3
-
27
-
-
84898984097
-
-
published correction appears
-
published correction appears in Nature. 2014;508(7496):420
-
(2014)
Nature
, vol.508
, Issue.7496
, pp. 420
-
-
-
28
-
-
84864255882
-
The origin and evolution of mutations in acute myeloid leukemia
-
Welch JS, Ley TJ, Link DC, et al. The origin and evolution of mutations in acute myeloid leukemia. Cell. 2012;150(2):264-278.
-
(2012)
Cell
, vol.150
, Issue.2
, pp. 264-278
-
-
Welch, J.S.1
Ley, T.J.2
Link, D.C.3
-
29
-
-
84921468426
-
Dnmt3a loss predisposes murine hematopoietic stem cells to malignant transformation
-
Mayle A, Yang L, Rodriguez B, et al. Dnmt3a loss predisposes murine hematopoietic stem cells to malignant transformation. Blood. 2015;125(4): 629-638.
-
(2015)
Blood
, vol.125
, Issue.4
, pp. 629-638
-
-
Mayle, A.1
Yang, L.2
Rodriguez, B.3
-
30
-
-
84888116023
-
Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo
-
Abdel-Waab O, Gao J, Adli M, et al. Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo. J Exp Med. 2013; 210(12):2641-2659.
-
(2013)
J Exp Med
, vol.210
, Issue.12
, pp. 2641-2659
-
-
Abdel-Waab, O.1
Gao, J.2
Adli, M.3
-
31
-
-
79960064353
-
Tet2 loss leads to increased hematopoietic stem cell selfrenewal and myeloid transformation
-
Moran-Crusio K, Reavie L, Shih A, et al. Tet2 loss leads to increased hematopoietic stem cell selfrenewal and myeloid transformation. Cancer Cell. 2011;20(1):11-24.
-
(2011)
Cancer Cell
, vol.20
, Issue.1
, pp. 11-24
-
-
Moran-Crusio, K.1
Reavie, L.2
Shih, A.3
-
32
-
-
84929162813
-
SRSF2 mutations contribute to myelodysplasia by mutant-specific effects on exon recognition
-
Kim E, Ilagan JO, Liang Y, et al. SRSF2 mutations contribute to myelodysplasia by mutant-specific effects on exon recognition. Cancer Cell. 2015; 27(5):617-630.
-
(2015)
Cancer Cell
, vol.27
, Issue.5
, pp. 617-630
-
-
Kim, E.1
Ilagan, J.O.2
Liang, Y.3
-
33
-
-
84902480315
-
Myelodysplastic syndromes are propagated by rare and distinct human cancer stem cells in vivo
-
Woll PS, Kjällquist U, Chowdhury O, et al. Myelodysplastic syndromes are propagated by rare and distinct human cancer stem cells in vivo. Cancer Cell. 2014;25(6):794-808.
-
(2014)
Cancer Cell
, vol.25
, Issue.6
, pp. 794-808
-
-
Woll, P.S.1
Kjällquist, U.2
Chowdhury, O.3
-
34
-
-
84928017682
-
-
published correction appears
-
[published correction appears in Cancer Cell. 2015;27(4):603-605
-
(2015)
Cancer Cell
, vol.27
, Issue.4
, pp. 603-605
-
-
-
35
-
-
84902468462
-
-
published correction appears
-
2014;25(6):861]
-
(2014)
Cancer Cell
, vol.25
, Issue.6
, pp. 861
-
-
-
36
-
-
84937904208
-
Clonal hematopoiesis of indeterminate potential and its distinction from myelodysplastic syndromes
-
Steensma DP, Bejar R, Jaiswal S, et al. Clonal hematopoiesis of indeterminate potential and its distinction from myelodysplastic syndromes. Blood. 2015;126(1):9-16.
-
(2015)
Blood
, vol.126
, Issue.1
, pp. 9-16
-
-
Steensma, D.P.1
Bejar, R.2
Jaiswal, S.3
-
37
-
-
84923222685
-
Preleukemia: The normal side of cancer
-
Shlush LI, Minden MD. Preleukemia: the normal side of cancer. Curr Opin Hematol. 2015;22(2): 77-84.
-
(2015)
Curr Opin Hematol
, vol.22
, Issue.2
, pp. 77-84
-
-
Shlush, L.I.1
Minden, M.D.2
-
38
-
-
84896109877
-
Protooncogenic role of mutant IDH2 in leukemia initiation and maintenance
-
Kats LM, Reschke M, Taulli R, et al. Protooncogenic role of mutant IDH2 in leukemia initiation and maintenance. Cell Stem Cell. 2014; 14(3):329-341.
-
(2014)
Cell Stem Cell
, vol.14
, Issue.3
, pp. 329-341
-
-
Kats, L.M.1
Reschke, M.2
Taulli, R.3
-
39
-
-
84994353833
-
Molecular profiling and relationship with clinical response in patients with IDH1 mutation-positive hematologic malignancies receiving AG-120, a first-in-class potent inhibitor of mutant IDH1, in addition to data from the completed dose escalation portion of the phase 1 study [abstract]
-
Abstract 1306
-
DiNardo C, de Botton S, Pollyea DA, et al. Molecular profiling and relationship with clinical response in patients with IDH1 mutation-positive hematologic malignancies receiving AG-120, a first-in-class potent inhibitor of mutant IDH1, in addition to data from the completed dose escalation portion of the phase 1 study [abstract]. Blood. 2015;126(23). Abstract 1306.
-
(2015)
Blood
, vol.126
, Issue.23
-
-
DiNardo, C.1
De Botton, S.2
Pollyea, D.A.3
-
40
-
-
0034665776
-
Isolation and characterization of hematopoietic progenitor/stem cells in 5q-deleted myelodysplastic syndromes: Evidence for involvement at the hematopoietic stem cell level
-
Nilsson L, Astrand-Grundström I, Arvidsson I, et al. Isolation and characterization of hematopoietic progenitor/stem cells in 5q-deleted myelodysplastic syndromes: evidence for involvement at the hematopoietic stem cell level. Blood. 2000;96(6):2012-2021.
-
(2000)
Blood
, vol.96
, Issue.6
, pp. 2012-2021
-
-
Nilsson, L.1
Astrand-Grundström, I.2
Arvidsson, I.3
-
41
-
-
78149454504
-
Next-generation sequencing of the TET2 gene in 355 MDS and CMML patients reveals lowabundance mutant clones with early origins, but indicates no definite prognostic value
-
Smith AE, Mohamedali AM, Kulasekararaj A, et al. Next-generation sequencing of the TET2 gene in 355 MDS and CMML patients reveals lowabundance mutant clones with early origins, but indicates no definite prognostic value. Blood. 2010;116(19):3923-3932.
-
(2010)
Blood
, vol.116
, Issue.19
, pp. 3923-3932
-
-
Smith, A.E.1
Mohamedali, A.M.2
Kulasekararaj, A.3
-
42
-
-
84959419840
-
Effect of lenalidomide treatment on clonal architecture of myelodysplastic syndromes without 5q deletion
-
Chesnais V, Renneville A, Toma A, et al. Effect of lenalidomide treatment on clonal architecture of myelodysplastic syndromes without 5q deletion. Blood. 2016;127(6):749-760.
-
(2016)
Blood
, vol.127
, Issue.6
, pp. 749-760
-
-
Chesnais, V.1
Renneville, A.2
Toma, A.3
-
43
-
-
84878900540
-
Clonal diversity of recurrently mutated genes in myelodysplastic syndromes
-
Walter MJ, Shen D, Shao J, et al. Clonal diversity of recurrently mutated genes in myelodysplastic syndromes. Leukemia. 2013;27(6):1275-1282.
-
(2013)
Leukemia
, vol.27
, Issue.6
, pp. 1275-1282
-
-
Walter, M.J.1
Shen, D.2
Shao, J.3
-
44
-
-
70449486011
-
Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis
-
Malcovati L, Della Porta MG, Pietra D, et al. Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis. Blood. 2009;114(17):3538-3545.
-
(2009)
Blood
, vol.114
, Issue.17
, pp. 3538-3545
-
-
Malcovati, L.1
Della Porta, M.G.2
Pietra, D.3
-
45
-
-
84863337617
-
Clonal architecture of secondary acute myeloid leukemia
-
Walter MJ, Shen D, Ding L, et al. Clonal architecture of secondary acute myeloid leukemia. N Engl J Med. 2012;366(12):1090-1098.
-
(2012)
N Engl J Med
, vol.366
, Issue.12
, pp. 1090-1098
-
-
Walter, M.J.1
Shen, D.2
Ding, L.3
-
46
-
-
78751644099
-
Genetic variegation of clonal architecture and propagating cells in leukaemia
-
Anderson K, Lutz C, van Delft FW, et al. Genetic variegation of clonal architecture and propagating cells in leukaemia. Nature. 2011;469(7330): 356-361.
-
(2011)
Nature
, vol.469
, Issue.7330
, pp. 356-361
-
-
Anderson, K.1
Lutz, C.2
Van Delft, F.W.3
-
47
-
-
84862776906
-
Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing
-
Ding L, Ley TJ, Larson DE, et al. Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing. Nature. 2012; 481(7382):506-510.
-
(2012)
Nature
, vol.481
, Issue.7382
, pp. 506-510
-
-
Ding, L.1
Ley, T.J.2
Larson, D.E.3
-
48
-
-
84864561961
-
Whole-genome sequencing of multiple myeloma from diagnosis to plasma cell leukemia reveals genomic initiating events, evolution, and clonal tides
-
Egan JB, Shi CX, Tembe W, et al. Whole-genome sequencing of multiple myeloma from diagnosis to plasma cell leukemia reveals genomic initiating events, evolution, and clonal tides. Blood. 2012; 120(5):1060-1066.
-
(2012)
Blood
, vol.120
, Issue.5
, pp. 1060-1066
-
-
Egan, J.B.1
Shi, C.X.2
Tembe, W.3
-
49
-
-
84863393080
-
Intratumor heterogeneity and branched evolution revealed by multiregion sequencing
-
Gerlinger M, Rowan AJ, Horswell S, et al. Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. N Engl J Med. 2012;366(10):883-892.
-
(2012)
N Engl J Med
, vol.366
, Issue.10
, pp. 883-892
-
-
Gerlinger, M.1
Rowan, A.J.2
Horswell, S.3
-
50
-
-
84874102335
-
Evolution and impact of subclonal mutations in chronic lymphocytic leukemia
-
Landau DA, Carter SL, Stojanov P, et al. Evolution and impact of subclonal mutations in chronic lymphocytic leukemia. Cell. 2013;152(4):714-726.
-
(2013)
Cell
, vol.152
, Issue.4
, pp. 714-726
-
-
Landau, D.A.1
Carter, S.L.2
Stojanov, P.3
-
51
-
-
78751661556
-
Evolution of human BCR-ABL1 lymphoblastic leukaemiainitiating cells
-
Notta F, Mullighan CG, Wang JC, et al. Evolution of human BCR-ABL1 lymphoblastic leukaemiainitiating cells. Nature. 2011;469(7330):362-367.
-
(2011)
Nature
, vol.469
, Issue.7330
, pp. 362-367
-
-
Notta, F.1
Mullighan, C.G.2
Wang, J.C.3
-
52
-
-
84877928684
-
Clonal architecture of chronic myelomonocytic leukemias
-
Itzykson R, Kosmider O, Renneville A, et al. Clonal architecture of chronic myelomonocytic leukemias. Blood. 2013;121(12):2186-2198.
-
(2013)
Blood
, vol.121
, Issue.12
, pp. 2186-2198
-
-
Itzykson, R.1
Kosmider, O.2
Renneville, A.3
|