589 related articles for article (PubMed ID: 19963117)
61. B-prolymphocytic leukaemia with t(11;14) revisited: a splenomegalic form of mantle cell lymphoma evolving with leukaemia.
Ruchlemer R; Parry-Jones N; Brito-Babapulle V; Attolico I; Wotherspoon AC; Matutes E; Catovsky D
Br J Haematol; 2004 May; 125(3):330-6. PubMed ID: 15086413
[TBL] [Abstract][Full Text] [Related]
62. Burkitt t(8;14)(q24;q32) and cryptic deletion in a CLL patient: report of a case and review of literature.
Reddy K; Satyadev R; Bouman D; Hibbard MK; Lu G; Paolo R
Cancer Genet Cytogenet; 2006 Apr; 166(1):12-21. PubMed ID: 16616107
[TBL] [Abstract][Full Text] [Related]
63. A case of hairy cell leukemia with CCND1-IGH@ translocation: indolent non-nodal mantle cell lymphoma revisited.
Chen D; Ketterling RP; Hanson CA; Colgan JP; Zent CS; Viswanatha DS
Am J Surg Pathol; 2011 Jul; 35(7):1080-4. PubMed ID: 21677543
[TBL] [Abstract][Full Text] [Related]
64. A new translocation t(11;13)(q13;q14) in a mature B-cell neoplasm.
Solé F; Salido M; Espinet B; Zamora L; Berlanga J; Domingo A
Haematologica; 2002 Jul; 87(7):777-8. PubMed ID: 12091133
[TBL] [Abstract][Full Text] [Related]
65. Two novel translocations disrupt the RUNX1 gene in acute myeloid leukemia.
Dai H; Xue Y; Pan J; Wu Y; Wang Y; Shen J; Zhang J
Cancer Genet Cytogenet; 2007 Sep; 177(2):120-4. PubMed ID: 17854666
[TBL] [Abstract][Full Text] [Related]
66. Telomeric IGH losses detectable by fluorescence in situ hybridization in chronic lymphocytic leukemia reflect somatic VH recombination events.
Wlodarska I; Matthews C; Veyt E; Pospisilova H; Catherwood MA; Poulsen TS; Vanhentenrijk V; Ibbotson R; Vandenberghe P; Morris TC; Alexander HD
J Mol Diagn; 2007 Feb; 9(1):47-54. PubMed ID: 17251335
[TBL] [Abstract][Full Text] [Related]
67. Spectral karyotyping and fluorescence in situ hybridization analyses identified a novel three-way translocation involving inversion 16 in therapy-related acute myeloid leukemia M4eo.
Ohsaka A; Otsubo K; Yokota H; Hisa T; Saito H; Kozaki T
Cancer Genet Cytogenet; 2008 Jul; 184(2):113-8. PubMed ID: 18617061
[TBL] [Abstract][Full Text] [Related]
68. Involvement of the BCL3 gene in two patients with chronic lymphocytic leukemia.
Yabumoto K; Ohno H; Doi S; Edamura S; Arita Y; Akasaka T; Matsumoto J; Kadowaki N; Fukuhara S; Okuma M
Int J Hematol; 1994 Apr; 59(3):211-8. PubMed ID: 8011990
[TBL] [Abstract][Full Text] [Related]
69. Cytogenetics of multiple myeloma: interpretation of fluorescence in situ hybridization results.
Harrison CJ; Mazzullo H; Cheung KL; Gerrard G; Jalali GR; Mehta A; Osier DG; Orchard KH
Br J Haematol; 2003 Mar; 120(6):944-52. PubMed ID: 12648063
[TBL] [Abstract][Full Text] [Related]
70. Disruption of the ETV6 gene as a consequence of a rare translocation (12;12)(p13;q13) in treatment-induced acute myeloid leukemia after breast cancer.
Manola KN; Georgakakos VN; Margaritis D; Stavropoulou C; Panos C; Kotsianidis I; Pantelias GE; Sambani C
Cancer Genet Cytogenet; 2008 Jan; 180(1):37-42. PubMed ID: 18068531
[TBL] [Abstract][Full Text] [Related]
71. Frequent occurrence of CCND1 deregulation in patients with early stages of plasma cell dyscrasia.
Miura K; Iida S; Hanamura I; Kato M; Banno S; Ishida T; Kusumoto S; Takeuchi G; Miwa H; Nitta M; Inagaki H; Eimoto T; Nomura K; Taniwaki M; Ueda R
Cancer Sci; 2003 Apr; 94(4):350-4. PubMed ID: 12824903
[TBL] [Abstract][Full Text] [Related]
72. Molecular cytogenetic aberrations in 21 Chinese patients with plasma cell leukemia.
Xu W; Li JY; Fan L; Chen LJ; Qiu HR; Qiu HX; Lu H
Int J Lab Hematol; 2009 Jun; 31(3):338-43. PubMed ID: 18284415
[TBL] [Abstract][Full Text] [Related]
73. t(9;11)(p22;p15) with NUP98-LEDGF fusion gene in pediatric acute myeloid leukemia.
Morerio C; Acquila M; Rosanda C; Rapella A; Tassano E; Micalizzi C; Panarello C
Leuk Res; 2005 Apr; 29(4):467-70. PubMed ID: 15725483
[TBL] [Abstract][Full Text] [Related]
74. An inv(16)(p13q22) positive acute myeloid leukaemia relapsing as acute precursor B-cell lymphoblastic leukaemia.
Boeckx N; van der Velden VH; Boogaerts M; Hagemeijer A; Vandenberghe P; van Dongen JJ
Haematologica; 2004 Aug; 89(8):ECR28. PubMed ID: 15339697
[TBL] [Abstract][Full Text] [Related]
75. Multicolor interphase cytogenetics for the study of plasma cell dyscrasias.
Sáez B; Martín-Subero JI; Odero MD; Prosper F; Cigudosa JC; Schoch R; Calasanz MJ; Siebert R
Oncol Rep; 2007 Nov; 18(5):1099-106. PubMed ID: 17914559
[TBL] [Abstract][Full Text] [Related]
76. Molecular classification of multiple myeloma: a distinct transcriptional profile characterizes patients expressing CCND1 and negative for 14q32 translocations.
Agnelli L; Bicciato S; Mattioli M; Fabris S; Intini D; Verdelli D; Baldini L; Morabito F; Callea V; Lombardi L; Neri A
J Clin Oncol; 2005 Oct; 23(29):7296-306. PubMed ID: 16129847
[TBL] [Abstract][Full Text] [Related]
77. Nucleolated variant of mantle cell lymphoma with leukemic manifestations mimicking prolymphocytic leukemia.
Wong KF; So CC; Chan JK
Am J Clin Pathol; 2002 Feb; 117(2):246-51. PubMed ID: 11865846
[TBL] [Abstract][Full Text] [Related]
78. De novo acute nonlymphoblastic leukemia (M5b) having a chromosomal 3;21 translocation with immunoglobin heavy-chain gene rearrangement.
Kaya H; Aoshima K; Okafuji K; Tanaka N; Ohtake S; Nakamura S; Matsuda T
Am J Hematol; 1996 Oct; 53(2):142-3. PubMed ID: 8892743
[No Abstract] [Full Text] [Related]
79. Indolent mantle cell lymphoma with nodal involvement and mutated immunoglobulin heavy chain genes.
Nodit L; Bahler DW; Jacobs SA; Locker J; Swerdlow SH
Hum Pathol; 2003 Oct; 34(10):1030-4. PubMed ID: 14608537
[TBL] [Abstract][Full Text] [Related]
80. Unusual case of leukemic mantle cell lymphoma with amplified CCND1/IGH fusion gene.
Gruszka-Westwood AM; Atkinson S; Summersgill BM; Shipley J; Elnenaei MO; Jain P; Hamoudi RA; Kaeda JS; Wotherspoon AC; Matutes E; Catovsky D
Genes Chromosomes Cancer; 2002 Feb; 33(2):206-12. PubMed ID: 11793447
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
