-
2
-
-
0036235310
-
Myeloid disorders with deletion of 5q as the sole karyotypic abnormality: The clinical and pathologic spectrum
-
Washington LBT, Doherty D, Glassman A, Martins J, Ibrahim S, Lai R. Myeloid disorders with deletion of 5q as the sole karyotypic abnormality: the clinical and pathologic spectrum. Leuk Lymphoma 2002;43:761-5.
-
(2002)
Leuk Lymphoma
, vol.43
, pp. 761-765
-
-
Washington, L.B.T.1
Doherty, D.2
Glassman, A.3
Martins, J.4
Ibrahim, S.5
Lai, R.6
-
3
-
-
0035160417
-
Molecular cytogenetic characterization of acute myeloid leukemia and myelodysplastic syndromes with multiple chromosome rearrangements
-
Lindvall C, Nordenskjold M, Porwit A, Bjorkholm M, Blennow E. Molecular cytogenetic characterization of acute myeloid leukemia and myelodysplastic syndromes with multiple chromosome rearrangements. Haematologica 2001;86:1158-64.
-
(2001)
Haematologica
, vol.86
, pp. 1158-1164
-
-
Lindvall, C.1
Nordenskjold, M.2
Porwit, A.3
Bjorkholm, M.4
Blennow, E.5
-
5
-
-
0035281739
-
Mutation with loss of heterozygosity of p53 are common in the related myelodysplasia and acute myeloid leukemia after exposure to alkylating agents and significantly associated with deletion or loss of 5q, a complex karyotype, and a poor prognosis
-
Christiansen DH, Andersen MK, Pedersen-Bjergaard J. Mutation with loss of heterozygosity of p53 are common in the related myelodysplasia and acute myeloid leukemia after exposure to alkylating agents and significantly associated with deletion or loss of 5q, a complex karyotype, and a poor prognosis. J Clin Oncol 2001;19:1405-13.
-
(2001)
J Clin Oncol
, vol.19
, pp. 1405-1413
-
-
Christiansen, D.H.1
Andersen, M.K.2
Pedersen-Bjergaard, J.3
-
6
-
-
0034237345
-
Interphase FISH for Y chromosome, VNTR polymorphisms, and RT-PCR for BCR-ABL in the monitoring of HLA-matched and mismatched transplants
-
Crescenzi B, Fizzotti M, Piattoni S, La Starza R, Matteucci C, Carotti A, et al. Interphase FISH for Y chromosome, VNTR polymorphisms, and RT-PCR for BCR-ABL in the monitoring of HLA-matched and mismatched transplants. Cancer Genet Cytogenet 2000;120:25.
-
(2000)
Cancer Genet Cytogenet
, vol.120
, pp. 25
-
-
Crescenzi, B.1
Fizzotti, M.2
Piattoni, S.3
La Starza, R.4
Matteucci, C.5
Carotti, A.6
-
7
-
-
0029759197
-
Succesful use of the same slide for consecutive fluorescence in situ hybridization (FISH) experiments
-
Dierlamm J, Wlodarska I, Michaux L, La Starza R, Zeller W, Mecucci C, et al. Succesful use of the same slide for consecutive fluorescence in situ hybridization (FISH) experiments. Genes Chromosomes Cancer 1996;16:261-4.
-
(1996)
Genes Chromosomes Cancer
, vol.16
, pp. 261-264
-
-
Dierlamm, J.1
Wlodarska, I.2
Michaux, L.3
La Starza, R.4
Zeller, W.5
Mecucci, C.6
-
8
-
-
0028928283
-
Myelodysplastic syndromes and acute myeloid leukemia with deletion. An entity characterized by specific dysgranulopoiesis and high incidence of P53 mutations
-
Lai JL, Preudhomme C, Zandecki M, Flactif M, Vanrumbeke M, Lepelley P, et al. Myelodysplastic syndromes and acute myeloid leukemia with deletion. An entity characterized by specific dysgranulopoiesis and high incidence of P53 mutations. Leukemia 1995;9:370-81.
-
(1995)
Leukemia
, vol.9
, pp. 370-381
-
-
Lai, J.L.1
Preudhomme, C.2
Zandecki, M.3
Flactif, M.4
Vanrumbeke, M.5
Lepelley, P.6
-
9
-
-
0035383839
-
Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis
-
Kolomietz E, Al-Maghrabi J, Brennan S, Karaskova J, Minkin S, Lipton J, et al. Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis. Blood 2001;97:3581-8.
-
(2001)
Blood
, vol.97
, pp. 3581-3588
-
-
Kolomietz, E.1
Al-Maghrabi, J.2
Brennan, S.3
Karaskova, J.4
Minkin, S.5
Lipton, J.6
-
10
-
-
0036736503
-
Large deletion 5′ to the ETO breakpoint are recurrent events in patients with t(8;21) acute myeloid leukemia
-
Godon C, Proffitt J, Dastugue N, Lafage-Pochitaloff M, Mozziconacci M-J, Talmant P, et al. Large deletion 5′ to the ETO breakpoint are recurrent events in patients with t(8;21) acute myeloid leukemia. Leukemia 2002;16:1752-4.
-
(2002)
Leukemia
, vol.16
, pp. 1752-1754
-
-
Godon, C.1
Proffitt, J.2
Dastugue, N.3
Lafage-Pochitaloff, M.4
Mozziconacci, M.-J.5
Talmant, P.6
-
11
-
-
0027182996
-
Rare occurrence of mutations of the FLR exon of the neurofibromatosis 1(NF1) gene in myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML)
-
Preudhomme C, Vachee A, Quesnel B, Wattel E, Cosson A, Fenaux P. Rare occurrence of mutations of the FLR exon of the neurofibromatosis 1(NF1) gene in myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). Leukemia 1993;7:1071.
-
(1993)
Leukemia
, vol.7
, pp. 1071
-
-
Preudhomme, C.1
Vachee, A.2
Quesnel, B.3
Wattel, E.4
Cosson, A.5
Fenaux, P.6
-
12
-
-
0029088646
-
Analysis of mutations of neurofibromatosis type 1 gene and N-ras gene in acute myelogenous leukemia
-
Lee YY, Kim WS, Bang YJ, Park S, Yoon WJ, Cho KS, et al. Analysis of mutations of neurofibromatosis type 1 gene and N-ras gene in acute myelogenous leukemia. Stem Cells 1995;13:556-63.
-
(1995)
Stem Cells
, vol.13
, pp. 556-563
-
-
Lee, Y.Y.1
Kim, W.S.2
Bang, Y.J.3
Park, S.4
Yoon, W.J.5
Cho, K.S.6
-
13
-
-
0028808203
-
Low frequency of RAS gene mutations and absence of mutations within the FLR exon of NF1 in patients with therapy-related leukemias
-
Borkhardt A, Brettreich S, Borkhardt AK, Repp R, Harbott J, Kreuder J, et al. Low frequency of RAS gene mutations and absence of mutations within the FLR exon of NF1 in patients with therapy-related leukemias. Leukemia 1995;9:1790-1.
-
(1995)
Leukemia
, vol.9
, pp. 1790-1791
-
-
Borkhardt, A.1
Brettreich, S.2
Borkhardt, A.K.3
Repp, R.4
Harbott, J.5
Kreuder, J.6
-
14
-
-
0032830638
-
Haploisufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukemia
-
Song WJ, Sullivan MG, Legare RD, Hutchings S, Tan X, Kufrin D, et al. Haploisufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukemia. Nat Genet 1999;23:166-75.
-
(1999)
Nat Genet
, vol.23
, pp. 166-175
-
-
Song, W.J.1
Sullivan, M.G.2
Legare, R.D.3
Hutchings, S.4
Tan, X.5
Kufrin, D.6
-
15
-
-
17044453376
-
Primary myelodysplastic syndrome with normal cytogenetics: Utility of "FISH panel testing" and M-FISH
-
Ketterling R, Wyatt W, VanWier SA, Law M, Hodnefield JM, Hanson CA, et al. Primary myelodysplastic syndrome with normal cytogenetics: utility of "FISH panel testing" and M-FISH. Leuk Res 2002;26:235-40.
-
(2002)
Leuk Res
, vol.26
, pp. 235-240
-
-
Ketterling, R.1
Wyatt, W.2
VanWier, S.A.3
Law, M.4
Hodnefield, J.M.5
Hanson, C.A.6
-
18
-
-
26544470092
-
Preferential suppression of trisomy 8 versus normal hematopoietic cell growth by autologous lymphocytes in patients with trisomy 8 myelodysplastic syndrome
-
Sloand E, Fuhrer M, Maciejewski JP, Johnson S, Barret AJ, Young NS. Preferential suppression of trisomy 8 versus normal hematopoietic cell growth by autologous lymphocytes in patients with trisomy 8 myelodysplastic syndrome. Leuk Res 2003;Suppl 1:S79.
-
(2003)
Leuk Res
, Issue.SUPPL. 1
-
-
Sloand, E.1
Fuhrer, M.2
Maciejewski, J.P.3
Johnson, S.4
Barret, A.J.5
Young, N.S.6
|