-
1
-
-
0032830638
-
Haploinsuffciency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia
-
Song, W.-J. et al. Haploinsuffciency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia. Nat. Genet. 23, 166-175 (1999).
-
(1999)
Nat. Genet.
, vol.23
, pp. 166-175
-
-
Song, W.-J.1
-
2
-
-
16544391755
-
Mutation of CEBPA in familial acute myeloid leukemia
-
Smith, M.L., Cavenagh, J.D., Lister, T.A. & Fitzgibbon, J. Mutation of CEBPA in familial acute myeloid leukemia. N. Engl. J. Med. 351, 2403-2407 (2004).
-
(2004)
N. Engl. J. Med.
, vol.351
, pp. 2403-2407
-
-
Smith, M.L.1
Cavenagh, J.D.2
Lister, T.A.3
Fitzgibbon, J.4
-
3
-
-
80053383273
-
Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia
-
Hahn, C.N. et al. Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia. Nat. Genet. 43, 1012-1017 (2011).
-
(2011)
Nat. Genet.
, vol.43
, pp. 1012-1017
-
-
Hahn, C.N.1
-
4
-
-
84863012056
-
Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature
-
Kazenwadel, J. et al. Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature. Blood 119, 1283-1291 (2012).
-
(2012)
Blood
, vol.119
, pp. 1283-1291
-
-
Kazenwadel, J.1
-
5
-
-
78650879044
-
Mutations in the 5′ UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2
-
Pippucci, T. et al. Mutations in the 5′ UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2. Am. J. Hum. Genet. 88, 115-120 (2011).
-
(2011)
Am. J. Hum. Genet.
, vol.88
, pp. 115-120
-
-
Pippucci, T.1
-
6
-
-
79959279291
-
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: Analysis of 78 patients from 21 families
-
Noris, P. et al. Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families. Blood 117, 6673-6680 (2011).
-
(2011)
Blood
, vol.117
, pp. 6673-6680
-
-
Noris, P.1
-
7
-
-
84860782889
-
Exome sequencing identifes autosomal-dominant SRP72 mutations associated with familial aplasia and myelodysplasia
-
Kirwan, M. et al. Exome sequencing identifes autosomal-dominant SRP72 mutations associated with familial aplasia and myelodysplasia. Am. J. Hum. Genet. 90, 888-892 (2012).
-
(2012)
Am. J. Hum. Genet.
, vol.90
, pp. 888-892
-
-
Kirwan, M.1
-
8
-
-
84884999671
-
A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia
-
Shah, S. et al. A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia. Nat. Genet. 45, 1226-1231 (2013).
-
(2013)
Nat. Genet.
, vol.45
, pp. 1226-1231
-
-
Shah, S.1
-
9
-
-
84899934875
-
Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547GA
-
Auer, F. et al. Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547GA. Leukemia 28, 1136-1138 (2014).
-
(2014)
Leukemia
, vol.28
, pp. 1136-1138
-
-
Auer, F.1
-
10
-
-
84874647204
-
The genomic landscape of hypodiploid acute lymphoblastic leukemia
-
Holmfeldt, L. et al. The genomic landscape of hypodiploid acute lymphoblastic leukemia. Nat. Genet. 45, 242-252 (2013).
-
(2013)
Nat. Genet.
, vol.45
, pp. 242-252
-
-
Holmfeldt, L.1
-
11
-
-
84876447944
-
Identifcation of TP53 as an acute lymphocytic leukemia susceptibility gene through exome sequencing
-
Powell, B.C. et al. Identifcation of TP53 as an acute lymphocytic leukemia susceptibility gene through exome sequencing. Pediatr. Blood Cancer 60, E1-E3 (2013).
-
(2013)
Pediatr. Blood Cancer
, vol.60
, pp. E1-E3
-
-
Powell, B.C.1
-
12
-
-
84920172497
-
Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity
-
19 September 2014
-
Zhang, M.Y. et al. Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity. Haematologica doi:10.3324/haematol.2014.113456 (19 September 2014).
-
Haematologica
-
-
Zhang, M.Y.1
-
13
-
-
84895920876
-
Steric mechanism of auto-inhibitory regulation of specifc and non-specifc DNA binding by the ETS transcriptional repressor ETV6
-
De, S. et al. Steric mechanism of auto-inhibitory regulation of specifc and non-specifc DNA binding by the ETS transcriptional repressor ETV6. J. Mol. Biol. 426, 1390-1406 (2014).
-
(2014)
J. Mol. Biol.
, vol.426
, pp. 1390-1406
-
-
De, S.1
-
14
-
-
84904815625
-
SWISS-MODEL: Modelling protein tertiary and quaternary structure using evolutionary information
-
Biasini, M. et al. SWISS-MODEL: modelling protein tertiary and quaternary structure using evolutionary information. Nucleic Acids Res. 42, W252-W258 (2014).
-
(2014)
Nucleic Acids Res.
, vol.42
, pp. W252-W258
-
-
Biasini, M.1
-
15
-
-
77953315305
-
DNA binding by the ETS protein TEL (ETV6) is regulated by autoinhibition and self-association
-
Green, S.M., Coyne, H.J. III, McIntosh, L.P. & Graves, B.J. DNA binding by the ETS protein TEL (ETV6) is regulated by autoinhibition and self-association. J. Biol. Chem. 285, 18496-18504 (2010).
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 18496-18504
-
-
Green, S.M.1
McIntosh, L.P.2
Graves, B.J.3
-
16
-
-
84863505218
-
Autoinhibition of ETV6 (TEL) DNA binding: Appended helices sterically block the ETS domain
-
Coyne, H.J. et al. Autoinhibition of ETV6 (TEL) DNA binding: appended helices sterically block the ETS domain. J. Mol. Biol. 421, 67-84 (2012).
-
(2012)
J. Mol. Biol.
, vol.421
, pp. 67-84
-
-
Coyne, H.J.1
-
17
-
-
0033517711
-
The leukemia-associated gene TEL encodes a transcription repressor which associates with SMRT and mSin3A
-
Chakrabarti, S.R. & Nucifora, G. The leukemia-associated gene TEL encodes a transcription repressor which associates with SMRT and mSin3A. Biochem. Biophys. Res. Commun. 264, 871-877 (1999).
-
(1999)
Biochem. Biophys. Res. Commun.
, vol.264
, pp. 871-877
-
-
Chakrabarti, S.R.1
Nucifora, G.2
-
18
-
-
33646846829
-
Identifcation of the nuclear localization motif in the ETV6 (TEL) protein
-
Park, H., Seo, Y., Kim, J.I., Kim, W. & Choe, S.Y. Identifcation of the nuclear localization motif in the ETV6 (TEL) protein. Cancer Genet. Cytogenet. 167, 117-121 (2006).
-
(2006)
Cancer Genet. Cytogenet.
, vol.167
, pp. 117-121
-
-
Park, H.1
Seo, Y.2
Kim, J.I.3
Kim, W.4
Choe, S.Y.5
-
19
-
-
0032873462
-
Both TEL and AML-1 contribute repression domains to the t(12;21) fusion protein
-
Fenrick, R. et al. Both TEL and AML-1 contribute repression domains to the t(12;21) fusion protein. Mol. Cell. Biol. 19, 6566-6574 (1999).
-
(1999)
Mol. Cell. Biol.
, vol.19
, pp. 6566-6574
-
-
Fenrick, R.1
-
20
-
-
0033858441
-
TEL, a putative tumor suppressor, modulates cell growth and cell morphology of Ras-transformed cells while repressing the transcription of stromelysin-1
-
Fenrick, R. et al. TEL, a putative tumor suppressor, modulates cell growth and cell morphology of Ras-transformed cells while repressing the transcription of stromelysin-1. Mol. Cell. Biol. 20, 5828-5839 (2000).
-
(2000)
Mol. Cell. Biol.
, vol.20
, pp. 5828-5839
-
-
Fenrick, R.1
-
21
-
-
0033570032
-
TEL is a sequence-specifc transcriptional repressor
-
Lopez, R.G. et al. TEL is a sequence-specifc transcriptional repressor. J. Biol. Chem. 274, 30132-30138 (1999).
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 30132-30138
-
-
Lopez, R.G.1
-
22
-
-
0032504190
-
The ets family member Tel binds to the Fli-1 oncoprotein and inhibits its transcriptional activity
-
Kwiatkowski, B.A. et al. The ets family member Tel binds to the Fli-1 oncoprotein and inhibits its transcriptional activity. J. Biol. Chem. 273, 17525-17530 (1998).
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 17525-17530
-
-
Kwiatkowski, B.A.1
-
23
-
-
0035421962
-
Polymerization of the SAM domain of TEL in leukemogenesis and transcriptional repression
-
Kim, C.A. et al. Polymerization of the SAM domain of TEL in leukemogenesis and transcriptional repression. EMBO J. 20, 4173-4182 (2001).
-
(2001)
EMBO J.
, vol.20
, pp. 4173-4182
-
-
Kim, C.A.1
-
24
-
-
0000418386
-
The TEL/ETV6 gene is required specifcally for hematopoiesis in the bone marrow
-
Wang, L.C. et al. The TEL/ETV6 gene is required specifcally for hematopoiesis in the bone marrow. Genes Dev. 12, 2392-2402 (1998).
-
(1998)
Genes Dev.
, vol.12
, pp. 2392-2402
-
-
Wang, L.C.1
-
25
-
-
4644274431
-
Tel/Etv6 is an essential and selective regulator of adult hematopoietic stem cell survival
-
Hock, H. et al. Tel/Etv6 is an essential and selective regulator of adult hematopoietic stem cell survival. Genes Dev. 18, 2336-2341 (2004).
-
(2004)
Genes Dev.
, vol.18
, pp. 2336-2341
-
-
Hock, H.1
-
26
-
-
84890409823
-
Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens
-
Pritchard, C.C. et al. Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens. J. Mol. Diagn. 16, 56-67 (2014).
-
(2014)
J. Mol. Diagn.
, vol.16
, pp. 56-67
-
-
Pritchard, C.C.1
-
27
-
-
84907987357
-
A new family with a germline ANKRD26 mutation and predisposition to myeloid malignancies
-
22 April 2014
-
Marquez, R. et al. A new family with a germline ANKRD26 mutation and predisposition to myeloid malignancies. Leuk. Lymphoma doi:10.3109/10428194. 2014.903476 (22 April 2014).
-
Leuk. Lymphoma
-
-
Marquez, R.1
-
28
-
-
78651486442
-
Densely interconnected transcriptional circuits control cell states in human hematopoiesis
-
Novershtern, N. et al. Densely interconnected transcriptional circuits control cell states in human hematopoiesis. Cell 144, 296-309 (2011).
-
(2011)
Cell
, vol.144
, pp. 296-309
-
-
Novershtern, N.1
-
29
-
-
84893875673
-
Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation
-
Bluteau, D. et al. Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation. J. Clin. Invest. 124, 580-591 (2014).
-
(2014)
J. Clin. Invest.
, vol.124
, pp. 580-591
-
-
Bluteau, D.1
-
31
-
-
84865459654
-
Recurrent R-spondin fusions in colon cancer
-
Seshagiri, S. et al. Recurrent R-spondin fusions in colon cancer. Nature 488, 660-664 (2012).
-
(2012)
Nature
, vol.488
, pp. 660-664
-
-
Seshagiri, S.1
-
32
-
-
84864255882
-
The origin and evolution of mutations in acute myeloid leukemia
-
Welch, J.S. et al. The origin and evolution of mutations in acute myeloid leukemia. Cell 150, 264-278 (2012).
-
(2012)
Cell
, vol.150
, pp. 264-278
-
-
Welch, J.S.1
-
33
-
-
84878900540
-
Clonal diversity of recurrently mutated genes in myelodysplastic syndromes
-
Walter, M.J. et al. Clonal diversity of recurrently mutated genes in myelodysplastic syndromes. Leukemia 27, 1275-1282 (2013).
-
(2013)
Leukemia
, vol.27
, pp. 1275-1282
-
-
Walter, M.J.1
-
34
-
-
84862907593
-
The genetic basis of early T-cell precursor acute lymphoblastic leukaemia
-
Zhang, J. et al. The genetic basis of early T-cell precursor acute lymphoblastic leukaemia. Nature 481, 157-163 (2012).
-
(2012)
Nature
, vol.481
, pp. 157-163
-
-
Zhang, J.1
-
35
-
-
79959794787
-
Clinical effect of point mutations in myelodysplastic syndromes
-
Bejar, R. et al. Clinical effect of point mutations in myelodysplastic syndromes. N. Engl. J. Med. 364, 2496-2506 (2011).
-
(2011)
N. Engl. J. Med.
, vol.364
, pp. 2496-2506
-
-
Bejar, R.1
-
36
-
-
84902147114
-
+ hematopoietic cells in myelodysplastic syndrome and gene mutation profles as prognostic markers
-
+ hematopoietic cells in myelodysplastic syndrome and gene mutation profles as prognostic markers. Proc. Natl. Acad. Sci. USA 111, 8589-8594 (2014).
-
(2014)
Proc. Natl. Acad. Sci. USA
, vol.111
, pp. 8589-8594
-
-
Xu, L.1
-
37
-
-
84862776906
-
Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing
-
Ding, L. et al. Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing. Nature 481, 506-510 (2012).
-
(2012)
Nature
, vol.481
, pp. 506-510
-
-
Ding, L.1
-
38
-
-
80053900941
-
Frequent pathway mutations of splicing machinery in myelodysplasia
-
Yoshida, K. et al. Frequent pathway mutations of splicing machinery in myelodysplasia. Nature 478, 64-69 (2011).
-
(2011)
Nature
, vol.478
, pp. 64-69
-
-
Yoshida, K.1
-
39
-
-
84868554484
-
Commonly altered genomic regions in acute myeloid leukemia are enriched for somatic mutations involved in chromatin remodeling and splicing
-
Dolnik, A. et al. Commonly altered genomic regions in acute myeloid leukemia are enriched for somatic mutations involved in chromatin remodeling and splicing. Blood 120, e83-e92 (2012).
-
(2012)
Blood
, vol.120
, pp. e83-e92
-
-
Dolnik, A.1
-
40
-
-
84905907421
-
ETV6 and signaling gene mutations are associated with secondary transformation of myelodysplastic syndromes to chronic myelomonocytic leukemia
-
Padron, E. et al. ETV6 and signaling gene mutations are associated with secondary transformation of myelodysplastic syndromes to chronic myelomonocytic leukemia. Blood 123, 3675-3677 (2014).
-
(2014)
Blood
, vol.123
, pp. 3675-3677
-
-
Padron, E.1
-
41
-
-
0036436878
-
Identifcation of an ETV6-ABL2 fusion transcript in combination with an ETV6 point mutation in a T-cell acute lymphoblastic leukaemia cell line
-
Griesinger, F., Janke, A., Podleschny, M. & Bohlander, S.K. Identifcation of an ETV6-ABL2 fusion transcript in combination with an ETV6 point mutation in a T-cell acute lymphoblastic leukaemia cell line. Br. J. Haematol. 119, 454-458 (2002).
-
(2002)
Br. J. Haematol.
, vol.119
, pp. 454-458
-
-
Griesinger, F.1
Janke, A.2
Podleschny, M.3
Bohlander, S.K.4
-
42
-
-
80052922387
-
Key pathways are frequently mutated in high-risk childhood acute lymphoblastic leukemia: A report from the Children's Oncology Group
-
Zhang, J. et al. Key pathways are frequently mutated in high-risk childhood acute lymphoblastic leukemia: a report from the Children's Oncology Group. Blood 118, 3080-3087 (2011).
-
(2011)
Blood
, vol.118
, pp. 3080-3087
-
-
Zhang, J.1
-
43
-
-
84907483015
-
ETV6 mutation in a cohort of 970 patients with hematologic malignancies
-
Wang, Q. et al. ETV6 mutation in a cohort of 970 patients with hematologic malignancies. Haematologica 99, e176-e178 (2014).
-
(2014)
Haematologica
, vol.99
, pp. e176-e178
-
-
Wang, Q.1
-
44
-
-
84892409192
-
Widespread genetic heterogeneity in multiple myeloma: Implications for targeted therapy
-
Lohr, J.G. et al. Widespread genetic heterogeneity in multiple myeloma: implications for targeted therapy. Cancer Cell 25, 91-101 (2014).
-
(2014)
Cancer Cell
, vol.25
, pp. 91-101
-
-
Lohr, J.G.1
-
45
-
-
84864258996
-
A landscape of driver mutations in melanoma
-
Hodis, E. et al. A landscape of driver mutations in melanoma. Cell 150, 251-263 (2012).
-
(2012)
Cell
, vol.150
, pp. 251-263
-
-
Hodis, E.1
-
46
-
-
77955084820
-
Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of non-syndromic hearing loss DFNB82
-
Walsh, T. et al. Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of non-syndromic hearing loss DFNB82. Am. J. Hum. Genet. 87, 90-94 (2010).
-
(2010)
Am. J. Hum. Genet.
, vol.87
, pp. 90-94
-
-
Walsh, T.1
-
47
-
-
84881193129
-
Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network
-
Gulsuner, S. et al. Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network. Cell 154, 518-529 (2013).
-
(2013)
Cell
, vol.154
, pp. 518-529
-
-
Gulsuner, S.1
-
48
-
-
81055126264
-
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identifed by massively parallel sequencing
-
Walsh, T. et al. Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identifed by massively parallel sequencing. Proc. Natl. Acad. Sci. USA 108, 18032-18037 (2011).
-
(2011)
Proc. Natl. Acad. Sci. USA
, vol.108
, pp. 18032-18037
-
-
Walsh, T.1
-
49
-
-
33750833078
-
Complete correction of murine Artemis immunodefciency by lentiviral vector-mediated gene transfer
-
Mostoslavsky, G., Fabian, A.J., Rooney, S., Alt, F.W. & Mulligan, R.C. Complete correction of murine Artemis immunodefciency by lentiviral vector-mediated gene transfer. Proc. Natl. Acad. Sci. USA 103, 16406-16411 (2006).
-
(2006)
Proc. Natl. Acad. Sci. USA
, vol.103
, pp. 16406-16411
-
-
Mostoslavsky, G.1
Fabian, A.J.2
Rooney, S.3
Alt, F.W.4
Mulligan, R.C.5
-
50
-
-
27144518462
-
Dose-dependent effects of the Notch ligand Delta1 on ex vivo differentiation and in vivo marrow repopulating ability of cord blood cells
-
Delaney, C., Varnum-Finney, B., Aoyama, K., Brashem-Stein, C. & Bernstein, I.D. Dose-dependent effects of the Notch ligand Delta1 on ex vivo differentiation and in vivo marrow repopulating ability of cord blood cells. Blood 106, 2693-2699 (2005).
-
(2005)
Blood
, vol.106
, pp. 2693-2699
-
-
Delaney, C.1
Varnum-Finney, B.2
Aoyama, K.3
Brashem-Stein, C.4
Bernstein, I.D.5
-
51
-
-
65449136284
-
TopHat: Discovering splice junctions with RNA-Seq
-
Trapnell, C., Pachter, L. & Salzberg, S.L. TopHat: discovering splice junctions with RNA-Seq. Bioinformatics 25, 1105-1111 (2009).
-
(2009)
Bioinformatics
, vol.25
, pp. 1105-1111
-
-
Trapnell, C.1
Pachter, L.2
Salzberg, S.L.3
-
52
-
-
84928987900
-
HTSeq-a Python framework to work with high-throughput sequencing data
-
25 September 2014
-
Anders, S., Pyl, P.T. & Huber, W. HTSeq-a Python framework to work with high-throughput sequencing data. Bioinformatics doi:10.1093/bioinformatics/btu638 (25 September 2014).
-
Bioinformatics
-
-
Anders, S.1
Pyl, P.T.2
Huber, W.3
-
53
-
-
75249087100
-
EdgeR: A Bioconductor package for differential expression analysis of digital gene expression data
-
Robinson, M.D., McCarthy, D.J. & Smyth, G.K. edgeR: a Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics 26, 139-140 (2010).
-
(2010)
Bioinformatics
, vol.26
, pp. 139-140
-
-
Robinson, M.D.1
McCarthy, D.J.2
Smyth, G.K.3
-
54
-
-
0037433040
-
Identifying differentially expressed genes using false discovery rate controlling procedures
-
Reiner, A., Yekutieli, D. & Benjamini, Y. Identifying differentially expressed genes using false discovery rate controlling procedures. Bioinformatics 19, 368-375 (2003).
-
(2003)
Bioinformatics
, vol.19
, pp. 368-375
-
-
Reiner, A.1
Yekutieli, D.2
Benjamini, Y.3
-
55
-
-
0035024021
-
Validating clustering for gene expression data
-
Yeung, K.Y., Haynor, D.R. & Ruzzo, W.L. Validating clustering for gene expression data. Bioinformatics 17, 309-318 (2001).
-
(2001)
Bioinformatics
, vol.17
, pp. 309-318
-
-
Yeung, K.Y.1
Haynor, D.R.2
Ruzzo, W.L.3
-
56
-
-
0037311919
-
TM4: A free, open-source system for microarray data management and analysis
-
Saeed, A.I. et al. TM4: a free, open-source system for microarray data management and analysis. Biotechniques 34, 374-378 (2003).
-
(2003)
Biotechniques
, vol.34
, pp. 374-378
-
-
Saeed, A.I.1
-
57
-
-
77953212372
-
Gene ontology analysis for RNA-seq: Accounting for selection bias
-
Young, M.D., Wakefeld, M.J., Smyth, G.K. & Oshlack, A. Gene ontology analysis for RNA-seq: accounting for selection bias. Genome Biol. 11, R14 (2010).
-
(2010)
Genome Biol.
, vol.11
, pp. R14
-
-
Young, M.D.1
Wakefeld, M.J.2
Smyth, G.K.3
Oshlack, A.4
-
58
-
-
84871485196
-
Impaired ribosomal subunit association in Shwachman-Diamond syndrome
-
Burwick, N., Coats, S.A., Nakamura, T. & Shimamura, A. Impaired ribosomal subunit association in Shwachman-Diamond syndrome. Blood 120, 5143-5152 (2012).
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(2012)
Blood
, vol.120
, pp. 5143-5152
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Burwick, N.1
Coats, S.A.2
Nakamura, T.3
Shimamura, A.4
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