-
1
-
-
0032907438
-
The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia
-
DOI 10.1038/5951
-
Draptchinskaia N, Gustavsson P, Andersson B, et al. The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia. Nat Genet. 1999;21(2):169-175. (Pubitemid 29070361)
-
(1999)
Nature Genetics
, vol.21
, Issue.2
, pp. 169-175
-
-
Draptchinskaia, N.1
Gustavsson, P.2
Andersson, B.3
Pettersson, M.4
Willig, T.-N.5
Dianzani, I.6
Ball, S.7
Tchernia, G.8
Klar, J.9
Matsson, H.10
Tentler, D.11
Mohandas, N.12
Carlsson, B.13
Dahl, N.14
-
2
-
-
33845303558
-
Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia
-
DOI 10.1086/510020
-
Gazda HT, Grabowska A, Merida-Long LB, et al. Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia. Am J Hum Genet. 2006;79(6):1110-1118. (Pubitemid 44868071)
-
(2006)
American Journal of Human Genetics
, vol.79
, Issue.6
, pp. 1110-1118
-
-
Gazda, H.T.1
Grabowska, A.2
Merida-Long, L.B.3
Latawiec, E.4
Schneider, H.E.5
Lipton, J.M.6
Vlachos, A.7
Atsidaftos, E.8
Ball, S.E.9
Orfali, K.A.10
Niewiadomska, E.11
Da, C.L.12
Tchernia, G.13
Niemeyer, C.14
Meerpohl, J.J.15
Stahl, J.16
Schratt, G.17
Glader, B.18
Backer, K.19
Wong, C.20
Nathan, D.G.21
Beggs, A.H.22
Sieff, C.A.23
more..
-
3
-
-
34848913619
-
Ribosomal protein S17 gene (RPS17) is mutated in Diamond-Blackfan anemia
-
DOI 10.1002/humu.20608
-
Cmejla R, Cmejlova J, Handrkova H, Petrak J, Pospisilova D. Ribosomal protein S17 gene (RPS17) is mutated in Diamond-Blackfan anemia. Hum Mutat. 2007;28(12):1178-1182. (Pubitemid 350250381)
-
(2007)
Human Mutation
, vol.28
, Issue.12
, pp. 1178-1182
-
-
Cmejla, R.1
Cmejlova, J.2
Handrkova, H.3
Petrak, J.4
Pospisilova, D.5
-
4
-
-
50649104789
-
Abnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemia
-
Farrar JE, Nater M, Caywood E, et al. Abnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemia. Blood. 2008;112(5):1582-1592.
-
(2008)
Blood
, vol.112
, Issue.5
, pp. 1582-1592
-
-
Farrar, J.E.1
Nater, M.2
Caywood, E.3
-
5
-
-
57649088933
-
Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients
-
Gazda HT, Sheen MR, Vlachos A, et al. Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients. Am J Hum Genet. 2008;83(6):769-780.
-
(2008)
Am J Hum Genet
, vol.83
, Issue.6
, pp. 769-780
-
-
Gazda, H.T.1
Sheen, M.R.2
Vlachos, A.3
-
6
-
-
78149440994
-
Ribosomal protein genes S10 and S26 are commonly mutated in Diamond-Blackfan anemia
-
abstract
-
Gazda HT, Sheen MR, Doherty L, et al. Ribosomal protein genes S10 and S26 are commonly mutated in Diamond-Blackfan anemia [abstract]. Blood. 2009;114(22):175.
-
(2009)
Blood
, vol.114
, Issue.22
, pp. 175
-
-
Gazda, H.T.1
Sheen, M.R.2
Doherty, L.3
-
7
-
-
76049086340
-
Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia
-
Doherty L, Sheen MR, Vlachos A, et al. Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia. Am J Hum Genet. 2010;86(2):222-228.
-
(2010)
Am J Hum Genet
, vol.86
, Issue.2
, pp. 222-228
-
-
Doherty, L.1
Sheen, M.R.2
Vlachos, A.3
-
8
-
-
79952747703
-
Array comparative genomic hybridization of ribosomal protein genes in Diamond-Blackfan anemia patients; evidence for three new DBA Genes, RPS8, RPS14 and RPL15, with large deletion or duplication
-
abstract
-
Gazda H, Landowski M, Buros C, et al. Array comparative genomic hybridization of ribosomal protein genes in Diamond-Blackfan anemia patients; evidence for three new DBA Genes, RPS8, RPS14 and RPL15, with large deletion or duplication [abstract]. Blood. 2010;116(21):1007.
-
(2010)
Blood
, vol.116
, Issue.21
, pp. 1007
-
-
Gazda, H.1
Landowski, M.2
Buros, C.3
-
9
-
-
48249117726
-
Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects
-
McGowan KA, Li JZ, Park CY, et al. Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects. Nat Genet. 2008;40(8):963- 970.
-
(2008)
Nat Genet
, vol.40
, Issue.8
, pp. 963-970
-
-
McGowan, K.A.1
Li, J.Z.2
Park, C.Y.3
-
10
-
-
77957967102
-
A transgenic mouse model demonstrates a dominant negative effect of a point mutation in the RPS19 gene associated with Diamond-Blackfan anemia
-
Devlin EE, Dacosta L, Mohandas N, Elliott G, Bodine DM. A transgenic mouse model demonstrates a dominant negative effect of a point mutation in the RPS19 gene associated with Diamond-Blackfan anemia. Blood. 2010;116(15): 2826-2835.
-
(2010)
Blood
, vol.116
, Issue.15
, pp. 2826-2835
-
-
Devlin, E.E.1
Dacosta, L.2
Mohandas, N.3
Elliott, G.4
Bodine, D.M.5
-
11
-
-
34848833327
-
Molecular basis of Diamond-Blackfan anemia: Structure and function analysis of RPS19
-
DOI 10.1093/nar/gkm626
-
Gregory LA, Aguissa-Toure AH, Pinaud N, Legrand P, Gleizes PE, Fribourg S. Molecular basis of Diamond-Blackfan anemia: structure and function analysis of RPS19. Nucleic Acids Res. 2007;35(17):5913-5921. (Pubitemid 47506305)
-
(2007)
Nucleic Acids Research
, vol.35
, Issue.17
, pp. 5913-5921
-
-
Gregory, L.A.1
Aguissa-Toure, A.-H.2
Pinaud, N.3
Legrand, P.4
Gleizes, P.-E.5
Fribourg, S.6
-
12
-
-
55549092113
-
A new database for ribosomal protein genes which are mutated in Diamond-Blackfan anemia
-
Boria I, Quarello P, Avondo F, et al. A new database for ribosomal protein genes which are mutated in Diamond-Blackfan anemia. Hum Mutat. 2008;29(11):E263-E270.
-
(2008)
Hum Mutat
, vol.29
, Issue.11
-
-
Boria, I.1
Quarello, P.2
Avondo, F.3
-
13
-
-
79952773882
-
Untangling the phenotypic heterogeneity of Diamond Blackfan anemia
-
Farrar JE, Dahl N. Untangling the phenotypic heterogeneity of Diamond Blackfan anemia. Semin Hematol. 2011;48(2):124-135.
-
(2011)
Semin Hematol
, vol.48
, Issue.2
, pp. 124-135
-
-
Farrar, J.E.1
Dahl, N.2
-
14
-
-
46749134457
-
RPS19 mutations in patients with Diamond- Blackfan anemia
-
Campagnoli MF, Ramenghi U, Armiraglio M, et al. RPS19 mutations in patients with Diamond- Blackfan anemia. Hum Mutat. 2008;29(7):911- 920.
-
(2008)
Hum Mutat
, vol.29
, Issue.7
, pp. 911-920
-
-
Campagnoli, M.F.1
Ramenghi, U.2
Armiraglio, M.3
-
15
-
-
10844220712
-
Nonsense-mediated and nonstop decay of ribosomal protein S19 mRNA in Diamond-Blackfan anemia
-
DOI 10.1002/humu.20117
-
Chatr-Aryamontri A, Angelini M, Garelli E, et al. Nonsense-mediated and nonstop decay of ribosomal protein S19 mRNA in Diamond-Blackfan anemia. Hum Mutat. 2004;24(6):526-533. (Pubitemid 39664607)
-
(2004)
Human Mutation
, vol.24
, Issue.6
, pp. 526-533
-
-
Chatr-Aryamontri, A.1
Angelini, M.2
Garelli, E.3
Tchernia, G.4
Ramenghi, U.5
Dianzani, I.6
Loreni, F.7
-
16
-
-
4944266230
-
RNA and protein evidence for haplo-insufficiency in Diamond-Blackfan anaemia patients with RPS19 mutations
-
DOI 10.1111/j.1365-2141.2004.05152.x
-
Gazda HT, Zhong R, Long L, et al. RNA and protein evidence for haplo-insufficiency in Diamond- Blackfan anaemia patients with RPS19 mutations. Br J Haematol. 2004;127(1):105-113. (Pubitemid 39331113)
-
(2004)
British Journal of Haematology
, vol.127
, Issue.1
, pp. 105-113
-
-
Gazda, H.T.1
Zhong, R.2
Long, L.3
Niewiadomska, E.4
Lipton, J.M.5
Ploszynska, A.6
Zaucha, J.M.7
Vlachos, A.8
Atsidaftos, E.9
Viskochil, D.H.10
Niemeyer, C.M.11
Meerpohl, J.J.12
Rokicka-Milewska, R.13
Pospisilova, D.14
Wiktor-Jedrzejczak, W.15
Nathan, D.G.16
Beggs, A.H.17
Sieff, C.A.18
-
17
-
-
0032231651
-
Identification of microdeletions spanning the Diamond-Blackfan anemia locus on 19q13 and evidence for genetic heterogeneity
-
DOI 10.1086/302100
-
Gustavsson P, Garelli E, Draptchinskaia N, et al. Identification of microdeletions spanning the Diamond- Blackfan anemia locus on 19q13 and evidence for genetic heterogeneity. Am J Hum Genet. 1998;63(5):1388-1395. (Pubitemid 30418535)
-
(1998)
American Journal of Human Genetics
, vol.63
, Issue.5
, pp. 1388-1395
-
-
Gustavsson, P.1
Garelli, E.2
Draptchinskaia, N.3
Ball, S.4
Willig, T.-N.5
Tentler, D.6
Dianzani, I.7
Punnett, H.H.8
Shafer, F.E.9
Cario, H.10
Ramenghi, U.11
Glomstein, A.12
Pfeiffer, R.A.13
Goringe, A.14
Olivieri, N.F.15
Smibert, E.16
Tchernia, G.17
Elinder, G.18
Dahl, N.19
-
18
-
-
55549145748
-
Multiplex ligation-dependent probe amplification enhances molecular diagnosis of Diamond-Blackfan anemia due to RPS19 deficiency
-
Quarello P, Garelli E, Brusco A, et al. Multiplex ligation-dependent probe amplification enhances molecular diagnosis of Diamond-Blackfan anemia due to RPS19 deficiency. Haematologica. 2008; 93(11):1748-1750.
-
(2008)
Haematologica
, vol.93
, Issue.11
, pp. 1748-1750
-
-
Quarello, P.1
Garelli, E.2
Brusco, A.3
-
19
-
-
79954672317
-
Genome structural variation discovery and genotyping
-
Alkan C, Coe BP, Eichler EE. Genome structural variation discovery and genotyping. Nat Rev Genet. 2011;12(5):363-376.
-
(2011)
Nat Rev Genet
, vol.12
, Issue.5
, pp. 363-376
-
-
Alkan, C.1
Coe, B.P.2
Eichler, E.E.3
-
20
-
-
33645284981
-
Improving clinical care and elucidating the pathophysiology of Diamond Blackfan anemia: An update from the Diamond Blackfan Anemia Registry
-
Lipton JM, Atsidaftos E, Zyskind I, Vlachos A. Improving clinical care and elucidating the pathophysiology of Diamond Blackfan anemia: an update from the Diamond Blackfan Anemia Registry. Pediatr Blood Cancer. 2006;46(5):558- 564.
-
(2006)
Pediatr Blood Cancer
, vol.46
, Issue.5
, pp. 558-564
-
-
Lipton, J.M.1
Atsidaftos, E.2
Zyskind, I.3
Vlachos, A.4
-
21
-
-
0034841762
-
The diamond blackfan anemia registry: Tool for investigating the epidemiology and biology of diamond-blackfan anemia
-
DOI 10.1097/00043426-200108000-00015
-
Vlachos A, Klein GW, Lipton JM. The Diamond Blackfan Anemia Registry: tool for investigating the epidemiology and biology of Diamond- Blackfan anemia. J Pediatr Hematol Oncol. 2001; 23(6):377-382. (Pubitemid 32845667)
-
(2001)
Journal of Pediatric Hematology/Oncology
, vol.23
, Issue.6
, pp. 377-382
-
-
Vlachos, A.1
Klein, G.W.2
Lipton, J.M.3
-
22
-
-
18144425478
-
A genome-wide scalable SNP genotyping assay using microarray technology
-
DOI 10.1038/ng1547
-
Gunderson KL, Steemers FJ, Lee G, Mendoza LG, Chee MS. A genome-wide scalable SNP genotyping assay using microarray technology. Nat Genet. 2005;37(5):549-554. (Pubitemid 40617286)
-
(2005)
Nature Genetics
, vol.37
, Issue.5
, pp. 549-554
-
-
Gunderson, K.L.1
Steemers, F.J.2
Lee, G.3
Mendoza, L.G.4
Chee, M.S.5
-
23
-
-
35948984173
-
PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
-
DOI 10.1101/gr.6861907
-
Wang K, Li M, Hadley D, et al. PennCNV: an integrated hidden Markov model designed for highresolution copy number variation detection in whole-genome SNP genotyping data. Genome Res. 2007;17(11):1665-1674. (Pubitemid 350074862)
-
(2007)
Genome Research
, vol.17
, Issue.11
, pp. 1665-1674
-
-
Wang, K.1
Li, M.2
Hadley, D.3
Liu, R.4
Glessner, J.5
Grant, S.F.A.6
Hakonarson, H.7
Bucan, M.8
-
24
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
DOI 10.1038/ng1416
-
Iafrate AJ, Feuk L, Rivera MN, et al. Detection of large-scale variation in the human genome. Nat Genet. 2004;36(9):949-951. (Pubitemid 39167488)
-
(2004)
Nature Genetics
, vol.36
, Issue.9
, pp. 949-951
-
-
Iafrate, A.J.1
Feuk, L.2
Rivera, M.N.3
Listewnik, M.L.4
Donahoe, P.K.5
Qi, Y.6
Scherer, S.W.7
Lee, C.8
-
25
-
-
33846867954
-
Human RPS19, the gene mutated in Diamond-Blackfan anemia, encodes a ribosomal protein required for the maturation of 40S ribosomal subunits
-
DOI 10.1182/blood-2006-07-038232
-
Flygare J, Aspesi A, Bailey JC, et al. Human RPS19, the gene mutated in Diamond-Blackfan anemia, encodes a ribosomal protein required for the maturation of 40S ribosomal subunits. Blood. 2007;109(3):980-986. (Pubitemid 46220642)
-
(2007)
Blood
, vol.109
, Issue.3
, pp. 980-986
-
-
Flygare, J.1
Aspesi, A.2
Bailey, J.C.3
Miyake, K.4
Caffrey, J.M.5
Karlsson, S.6
Ellis, S.R.7
-
26
-
-
78149361715
-
Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond-Blackfan anaemia
-
Wat MJ, Enciso VB, Wiszniewski W, et al. Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond-Blackfan anaemia. J Med Genet. 2010;47(11): 777-781.
-
(2010)
J Med Genet
, vol.47
, Issue.11
, pp. 777-781
-
-
Wat, M.J.1
Enciso, V.B.2
Wiszniewski, W.3
-
27
-
-
77956380533
-
Functional dichotomy of ribosomal proteins during the synthesis of mammalian 40S ribosomal subunits
-
O'Donohue MF, Choesmel V, Faubladier M, Fichant G, Gleizes PE. Functional dichotomy of ribosomal proteins during the synthesis of mammalian 40S ribosomal subunits. J Cell Biol. 2010; 190(5):853-866.
-
(2010)
J Cell Biol
, vol.190
, Issue.5
, pp. 853-866
-
-
O'Donohue, M.F.1
Choesmel, V.2
Faubladier, M.3
Fichant, G.4
Gleizes, P.E.5
-
28
-
-
79952752319
-
New determination method for extensive gene deletions in Diamond-Blackfan anemia
-
abstract
-
Kuramitsu M, Morio T, Takagi M, et al. New determination method for extensive gene deletions in Diamond-Blackfan anemia [abstract]. Blood. 2010;116(21):4231.
-
(2010)
Blood
, vol.116
, Issue.21
, pp. 4231
-
-
Kuramitsu, M.1
Morio, T.2
Takagi, M.3
-
29
-
-
13044266374
-
Mutations in ribosomal protein S19 gene and Diamond Blackfan anemia: Wide variations in phenotypic expression
-
Willig TN, Draptchinskaia N, Dianzani I, et al. Mutations in ribosomal protein S19 gene and Diamond Blackfan anemia: wide variations in phenotypic expression. Blood. 1999;94(12):4294-4306.
-
(1999)
Blood
, vol.94
, Issue.12
, pp. 4294-4306
-
-
Willig, T.N.1
Draptchinskaia, N.2
Dianzani, I.3
-
30
-
-
77956024596
-
Mutations in the ribosomal protein genes in Japanese patients with Diamond-Blackfan anemia
-
Konno Y, Toki T, Tandai S, et al. Mutations in the ribosomal protein genes in Japanese patients with Diamond-Blackfan anemia. Haematologica. 2010;95(8):1293-1299.
-
(2010)
Haematologica.
, vol.95
, Issue.8
, pp. 1293-1299
-
-
Konno, Y.1
Toki, T.2
Tandai, S.3
-
31
-
-
77649098172
-
A novel initiation codon mutation in the ribosomal protein S17 gene (RPS17) in a patient with Diamond-Blackfan anemia
-
Song MJ, Yoo EH, Lee KO, et al. A novel initiation codon mutation in the ribosomal protein S17 gene (RPS17) in a patient with Diamond-Blackfan anemia. Pediatr Blood Cancer. 2010;54(4):629- 631.
-
(2010)
Pediatr Blood Cancer
, vol.54
, Issue.4
, pp. 629-631
-
-
Song, M.J.1
Yoo, E.H.2
Lee, K.O.3
-
32
-
-
34848904050
-
Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardation
-
DOI 10.1086/521274
-
Wagenstaller J, Spranger S, Lorenz-Depiereux B, et al. Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardation. Am J Hum Genet. 2007;81(4):768-779. (Pubitemid 47596544)
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.4
, pp. 768-779
-
-
Wagenstaller, J.1
Spranger, S.2
Lorenz-Depiereux, B.3
Kazmierczak, B.4
Nathrath, M.5
Wahl, D.6
Heye, B.7
Glaser, D.8
Liebscher, V.9
Meitinger, T.10
Strom, T.M.11
-
33
-
-
20544462642
-
Segmental duplications and copy-number variation in the human genome
-
DOI 10.1086/431652
-
Sharp AJ, Locke DP, McGrath SD, et al. Segmental duplications and copy-number variation in the human genome. Am J Hum Genet. 2005;77(1): 78-88. (Pubitemid 40848038)
-
(2005)
American Journal of Human Genetics
, vol.77
, Issue.1
, pp. 78-88
-
-
Sharp, A.J.1
Locke, D.P.2
McGrath, S.D.3
Cheng, Z.4
Bailey, J.A.5
Vallente, R.U.6
Pertz, L.M.7
Clark, R.A.8
Schwartz, S.9
Segraves, R.10
Oseroff, V.V.11
Albertson, D.G.12
Pinkel, D.13
Eichler, E.E.14
-
34
-
-
33746513094
-
Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome
-
DOI 10.1086/505653
-
Locke DP, Sharp AJ, McCarroll SA, et al. Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome. Am J Hum Genet. 2006;79(2): 275-290. (Pubitemid 44141826)
-
(2006)
American Journal of Human Genetics
, vol.79
, Issue.2
, pp. 275-290
-
-
Locke, D.P.1
Sharp, A.J.2
McCarroll, S.A.3
McGrath, S.D.4
Newman, T.L.5
Cheng, Z.6
Schwartz, S.7
Albertson, D.G.8
Pinkel, D.9
Altshuler, D.M.10
Eichler, E.E.11
-
35
-
-
35748971743
-
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: Implications for association studies of complex diseases
-
de Smith AJ, Tsalenko A, Sampas N, et al. Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases. Hum Mol Genet. 2007;16(23):2783- 2794.
-
(2007)
Hum Mol Genet
, vol.16
, Issue.23
, pp. 2783-2794
-
-
De Smith, A.J.1
Tsalenko, A.2
Sampas, N.3
-
36
-
-
0036796620
-
Identification and analysis of over 2000 ribosomal protein pseudogenes in the human genome
-
DOI 10.1101/gr.331902
-
Zhang Z, Harrison P, Gerstein M. Identification and analysis of over 2000 ribosomal protein pseudogenes in the human genome. Genome Res. 2002;12(10):1466-1482. (Pubitemid 35189531)
-
(2002)
Genome Research
, vol.12
, Issue.10
, pp. 1466-1482
-
-
Zhang, Z.1
Harrison, P.2
Gerstein, M.3
-
37
-
-
50649096622
-
The role of human ribosomal proteins in the maturation of rRNA and ribosome production
-
Robledo S, Idol RA, Crimmins DL, Ladenson JH, Mason PJ, Bessler M. The role of human ribosomal proteins in the maturation of rRNA and ribosome production. RNA. 2008;14(9):1918-1929.
-
(2008)
RNA
, vol.14
, Issue.9
, pp. 1918-1929
-
-
Robledo, S.1
Idol, R.A.2
Crimmins, D.L.3
Ladenson, J.H.4
Mason, P.J.5
Bessler, M.6
-
38
-
-
77951702768
-
Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis
-
Conlin LK, Thiel BD, Bonnemann CG, et al. Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis. Hum Mol Genet. 2010; 19(7):1263-1275.
-
(2010)
Hum Mol Genet
, vol.19
, Issue.7
, pp. 1263-1275
-
-
Conlin, L.K.1
Thiel, B.D.2
Bonnemann, C.G.3
-
39
-
-
79952758947
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5q-myelodysplastic syndrome in one of 23 children lacking a known ribosomal gene mutation, masquerading as Diamond Blackfan anemia (DBA) and responding to lenalidomide
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abstract
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Vlachos A, Farrar J, Atsidaftos E, et al. 5q-myelodysplastic syndrome in one of 23 children lacking a known ribosomal gene mutation, masquerading as Diamond Blackfan anemia (DBA) and responding to lenalidomide [abstract]. Blood. 2010;116(21):LBA-2.
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(2010)
Blood
, vol.116
, Issue.21
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Vlachos, A.1
Farrar, J.2
Atsidaftos, E.3
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