131 related articles for article (PubMed ID: 16364771)
1. The translocation (4;12)(q31;q21) in myelofibrosis associated with myelodysplastic syndrome: impact of the 12q21 breakpoint.
Nunoda K; Sashida G; Ohyashiki K; Kodama A; Fukutake K
Cancer Genet Cytogenet; 2006 Jan; 164(1):90-1. PubMed ID: 16364771
[No Abstract] [Full Text] [Related]
2. Prevalence, breakpoint distribution, and clinical correlates of t(5;12).
Greipp PT; Dewald GW; Tefferi A
Cancer Genet Cytogenet; 2004 Sep; 153(2):170-2. PubMed ID: 15350308
[TBL] [Abstract][Full Text] [Related]
3. Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders.
Reddy KS; Richkind K; Ross M; Seirra R
Cancer Genet Cytogenet; 2005 Feb; 157(1):70-3. PubMed ID: 15676151
[TBL] [Abstract][Full Text] [Related]
4. Trisomy 14, deletion 20q and t(3;3) (q21;q26) in a case of myelodysplastic syndrome with myelofibrosis.
Kwong YL; Wan TS; Liang R; Chan LC
Clin Lab Haematol; 1994 Mar; 16(1):79-84. PubMed ID: 8039350
[TBL] [Abstract][Full Text] [Related]
5. A novel t(1;12)(q21;q24) in a patient with myelodysplastic syndrome.
Park TS; Lee SG; Song J; Kim JS; Choi JR
Ann Hematol; 2010 May; 89(5):513-6. PubMed ID: 19697027
[No Abstract] [Full Text] [Related]
6. A case of atypical myelodysplastic syndrome with a novel reciprocal translocation t(1;12)(q21;p13).
Sánchez J; Serrano J; Román J; García JM; Nomdedéu J; Torres A
Haematologica; 2000 Apr; 85(4):434-5. PubMed ID: 10756375
[No Abstract] [Full Text] [Related]
7. [A case of atypical myelodysplastic syndrome with eosinophilia and complex cytogenetic changes t(3; 12)(q21; p13); t(16; 17); (q24; q12)].
Abdulkadyrov KM; Gritsaev SV; Rukavitsyn OA; Martynkevich IS; Tiranova SA; Balashova VA; Blinov MN; Kharchenko MF
Ter Arkh; 2002; 74(7):70-2. PubMed ID: 12181842
[No Abstract] [Full Text] [Related]
8. Myelodysplastic syndrome with an unbalanced 1;16 translocation in a case of early age of onset.
Dean S; Mohamed AN
Am J Hematol; 2007 May; 82(5):396-9. PubMed ID: 17099874
[TBL] [Abstract][Full Text] [Related]
9. Translocation (10;21)(q21;q22) in myelodysplastic syndrome.
Rashaan Z; Ito Y; Takaku T; Toyotake J; Miyazawa K; Kodama A; Ohyashiki K
Cancer Genet Cytogenet; 2007 Feb; 173(1):81-2. PubMed ID: 17284376
[No Abstract] [Full Text] [Related]
10. Myelodysplastic syndrome associated with increased bone marrow fibrosis and translocation (5;12)(q33;p12.3).
Lerza R; Castello G; Sessarego M; Cavallini D; Pannacciulli I
Br J Haematol; 1992 Oct; 82(2):476-7. PubMed ID: 1419834
[No Abstract] [Full Text] [Related]
11. Trisomy 13 in a patient with idiopathic myelofibrosis.
Gozzetti A; Crupi R; Tozzuoli D; Fabbri A; Bocchia M; Lauria F
Cancer Genet Cytogenet; 2005 Jan; 156(2):185. PubMed ID: 15642403
[No Abstract] [Full Text] [Related]
12. [A case of myelodysplastic syndrome with abnormal chromosome t (3;4), proliferation of megakaryocytes and myelofibrosis, transition to overt leukemia].
Nehashi Y; Iwabuchi H; Tsuda A; Kawanishi Y; Tauchi T; Kawaguchi M; Oyashiki K; Sotoyama K
Nihon Naika Gakkai Zasshi; 1991 May; 80(5):759-60. PubMed ID: 1875112
[No Abstract] [Full Text] [Related]
13. A therapy resistant myelodysplastic syndrome characterized by the presence of the rare reciprocal translocation t(3;12)(q26.2;p13).
Orciuolo E; Buda G; Cecconi N; Galimberti S; Petrini M
Leuk Res; 2007 Nov; 31(11):1599-600. PubMed ID: 17210176
[No Abstract] [Full Text] [Related]
14. A second case of myelodysplastic syndrome with t(9;12)(q22;p12).
Mahmoodi M; Swami VK; Besa EC; Punnett HH
Cancer Genet Cytogenet; 2005 Mar; 157(2):187-8. PubMed ID: 15721645
[No Abstract] [Full Text] [Related]
15. Myelodysplastic syndrome accompanied by basophilia and eosinophilia with t(5;12)(q31;p13).
Katsura Y; Suzukawa K; Nanmoku T; Nemoto N; Machino T; Obara N; Okoshi Y; Mukai HY; Hasegawa Y; Kojima H; Kawakami Y; Nagasawa T
Cancer Genet Cytogenet; 2007 Oct; 178(1):85-8. PubMed ID: 17889716
[No Abstract] [Full Text] [Related]
16. Cryptic deletion of EGR1 in association with a novel balanced t(5;22)(q31;q11.2) in a patient with myelodysplastic syndrome.
Hoffman MW; Janney S; Batanian JR
Cancer Genet Cytogenet; 2009 Jun; 191(2):106-8. PubMed ID: 19446747
[TBL] [Abstract][Full Text] [Related]
17. Pseudoreticulocytosis in a case of myelodysplastic syndrome with translocation t(1;14) (q42;q32).
de Pree C; Cabrol C; Frossard JL; Beris P
Semin Hematol; 1995 Jul; 32(3):232-6. PubMed ID: 7570066
[No Abstract] [Full Text] [Related]
18. [Myelodysplastic syndrome showing translocation (1 ; 7) and translocation (3 ; 3)].
Kishimoto Y; Tamai T; Ohga S; Nagano T; Kawamura H; Kitajima H; Fujimoto M; Kimura T; Fujitake H; Yasunaga K
Rinsho Ketsueki; 1988 May; 29(5):743-7. PubMed ID: 3216503
[No Abstract] [Full Text] [Related]
19. A novel translocation der(4)t(1;4)(q21;q35) and a marker chromosome in a case of myelodysplastic syndrome.
Vundinti BR; Madkaikar M; Kerketta L; Jijina F; Ghosh K; Mohanty D; Jijina F
Cancer Genet Cytogenet; 2003 Jul; 144(2):175-6. PubMed ID: 12850381
[No Abstract] [Full Text] [Related]
20. A novel t(11;14)(q23;q32) in a case of myelodysplastic syndrome.
Yujiri T; Miyazaki M; Imoto S
Cancer Genet Cytogenet; 2009 Jan; 188(2):124-5. PubMed ID: 19100518
[No Abstract] [Full Text] [Related]
[Next] [New Search]
