148 related articles for article (PubMed ID: 19697027)
1. 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]
2. A novel gene, MDS2, is fused to ETV6/TEL in a t(1;12)(p36.1;p13) in a patient with myelodysplastic syndrome.
Odero MD; Vizmanos JL; Román JP; Lahortiga I; Panizo C; Calasanz MJ; Zeleznik-Le NJ; Rowley JD; Novo FJ
Genes Chromosomes Cancer; 2002 Sep; 35(1):11-9. PubMed ID: 12203785
[TBL] [Abstract][Full Text] [Related]
3. [A novel translocation t(1;18)(p31;p11) in a patient with myelodysplastic syndrome].
Du B; Wu YF; Pan JL; Xue YQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):74-5. PubMed ID: 15696486
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. A case of atypical myelodysplastic syndrome with micromegakaryocytes, normal platelet count, and t(3;12)(q21;p13) with inv(3)(q21q26).
Schnittger S; Schoch C; Streubel B; Hinrichs HF; Otremba B; Parwaresch R; Fonatsch C
Genes Chromosomes Cancer; 1997 Nov; 20(3):292-8. PubMed ID: 9365837
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. [Dual-color FISH study on myelodysplastic syndrome with 1;7 translocation].
Shen Y; Xue Y; Li J; Pan J; Wu Y; Guo Y; Lu D
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug; 19(4):313-6. PubMed ID: 12170469
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. MEL1S, not MEL1, is overexpressed in myelodysplastic syndromes patients with t(1;3)(p36;q21).
Xiao Z; Zhang M; Liu X; Zhang Y; Yang L; Hao Y
Leuk Res; 2006 Mar; 30(3):332-4. PubMed ID: 16102824
[TBL] [Abstract][Full Text] [Related]
10. Derivative (1)t(1;16)(p11;p11.1) in myelodysplastic syndrome: a case report and review of the literature.
Lunghi M; Casorzo L; De Paoli L; Riccomagno P; Rossi D; Gaidano G
Cancer Genet Cytogenet; 2010 Jan; 196(1):89-92. PubMed ID: 19963141
[TBL] [Abstract][Full Text] [Related]
11. Gain of 1q in pediatric myelodysplastic syndromes.
Morerio C; Rapella A; Tassano E; Lanino E; Micalizzi C; Rosanda C; Panarello C
Leuk Res; 2006 Nov; 30(11):1437-41. PubMed ID: 16472857
[TBL] [Abstract][Full Text] [Related]
12. Novel constitutional translocations t(3;5)(p25;q22) and t(1;14)(p31;q21) in patients with acute leukemia.
Panani AD; Pappa V; Raptis SA
Ann Hematol; 2004 Mar; 83(3):156-9. PubMed ID: 15064864
[TBL] [Abstract][Full Text] [Related]
13. Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip--palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24).
Callier P; Faivre L; Marle N; Thauvin-Robinet C; Mosca AL; Masurel-Paulet A; Borgnon J; Falcon-Eicher S; Danino A; Malka G; Le Merrer M; Huet F; Mugneret F
Eur J Med Genet; 2007; 50(6):455-64. PubMed ID: 17720646
[TBL] [Abstract][Full Text] [Related]
14. Novel chromosomal translocations in multiple myeloma: t(13;16)(q14;q24) and t(1;15)(q10;q26).
Akalin I; Kutlay NY; Ilhan O; Tukun A
Int J Lab Hematol; 2007 Jun; 29(3):215-20. PubMed ID: 17474900
[TBL] [Abstract][Full Text] [Related]
15. [Terminal 1q deletion by translocation t(1;20)pat, confirmed by in situ hybridization].
López-Ginés C; Gil-Benso R; Gregori-Romero MA; Paredes-Cencillo C; Castelló-Pomares M; Llombart-Bosch A
An Esp Pediatr; 1998 Mar; 48(3):309-11. PubMed ID: 9608096
[No Abstract] [Full Text] [Related]
16. A case of myelodysplastic syndrome with erythroid hypoplasia associated with a familial translocation t(3;14)(p21.1;q24.1).
Dinçol G; Oztürk S; Palanduz S; Tutkan G; Yildirim N; Ayer M; Güvenç S
Am J Hematol; 2006 Nov; 81(11):883-7. PubMed ID: 16888788
[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. 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]
19. Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis.
Lestou VS; Ludkovski O; Connors JM; Gascoyne RD; Lam WL; Horsman DE
Genes Chromosomes Cancer; 2003 Apr; 36(4):375-81. PubMed ID: 12619161
[TBL] [Abstract][Full Text] [Related]
20. Therapy-related myelodysplastic syndrome with der(17)t(12;17)(q13;p13) as a new recurrent cytogenetic abnormality after treatment for chronic lymphocytic leukemia.
Park TS; Cheong JW; Song J; Choi JR
Leuk Res; 2009 Jul; 33(7):1001-4. PubMed ID: 19155067
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
