125 related articles for article (PubMed ID: 16019491)
1. Biphenotypic acute leukemia with t(15;17).
Scolnik MP; Aranguren PN; Cuello MT; Palacios MF; Sanjurjo J; Giunta M; Bracco MM; Acevedo S
Leuk Lymphoma; 2005 Apr; 46(4):607-10. PubMed ID: 16019491
[TBL] [Abstract][Full Text] [Related]
2. Acute promyelocytic leukemia: the study of t(15;17) translocation by fluorescent in situ hybridization, reverse transcriptase-polymerase chain reaction and cytogenetic techniques.
Chauffaille ML; Figueiredo MS; Beltrani R; Antunes SV; Yamamoto M; Kerbauy J
Braz J Med Biol Res; 2001 Jun; 34(6):735-43. PubMed ID: 11378661
[TBL] [Abstract][Full Text] [Related]
3. [Detection of PML/RARA rearrangement by reverse transcriptase-PCR and sequencing in a case of microgranular acute promyelocytic leukemia lacking t(15;17) on karyotype and FISH].
Kim KE; Woo KS; Kim SH; Han JY
Korean J Lab Med; 2009 Oct; 29(5):379-83. PubMed ID: 19893344
[TBL] [Abstract][Full Text] [Related]
4. Coexistence of tetrasomy 8 and trisomy 8 in acute promyelocytic leukemia (AML-M3) with t(15;17)(q22;q12).
Wang HP; Li GX; Qiao ZH; Ren WY; Wang HW
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2004 Aug; 12(4):406-10. PubMed ID: 15363120
[TBL] [Abstract][Full Text] [Related]
5. Identification of PML-RARA rearrangement by RT-PCR and sequencing in an acute promyelocytic leukemia without t(15;17) on G-banding and FISH.
Han JY; Kim KE; Kim KH; Park JI; Kim JS
Leuk Res; 2007 Feb; 31(2):239-43. PubMed ID: 16797070
[TBL] [Abstract][Full Text] [Related]
6. A Paediatric Acute Promyelocytic Leukaemia Patient Harbouring a Cryptic PML-RARA Insertion due to a Complex Structural Chromosome 17 Rearrangement.
El-Hajj Ghaoui R; St Heaps L; Hung D; Nagabushan S; Harris C; Mirochnik O; Sharma P; Kellie SJ; Wright DC
Cytogenet Genome Res; 2017; 153(4):181-189. PubMed ID: 29550828
[TBL] [Abstract][Full Text] [Related]
7. Late-appearing Philadelphia chromosome in childhood acute myeloid leukemia.
Shah N; Leaker MT; Teshima I; Baruchel S; Abdelhaleem M; Ye CC
Pediatr Blood Cancer; 2008 May; 50(5):1052-3. PubMed ID: 18213712
[TBL] [Abstract][Full Text] [Related]
8. Cytogenetic, fluorescent in situ hybridization & reverse transcriptase-polymerase chain reaction analysis in acute promyelocytic leukaemia patients.
Shivakumar S; Poonkhuzhali B; Gunasekaran S; Srivastava A; Chandy M
Indian J Med Res; 2002 Feb; 115():59-67. PubMed ID: 12138666
[TBL] [Abstract][Full Text] [Related]
9. Cytogenetics and fluorescence in-situ hybridization in detection of hematological malignancies.
Frenny VJ; Antonella Z; Luisa A; Shah AD; Sheth JJ; Rocchi M
Indian J Cancer; 2003; 40(4):135-9. PubMed ID: 14716109
[TBL] [Abstract][Full Text] [Related]
10. [Chromosome t (8; 21) and t (15; 17) in a patient with acute myeloid leukemia].
Gao Y; Wang C; Xu L; Cao Q; Zhu Y; Cai Q; Yan S; Yang X
Zhonghua Xue Ye Xue Za Zhi; 2001 Feb; 22(2):94-5. PubMed ID: 11877058
[TBL] [Abstract][Full Text] [Related]
11. Mixed Phenotype Acute Leukemia with t(12;17)(p13;q21)/TAF15-ZNF384 and Other Chromosome Abnormalities.
Yamamoto K; Kawamoto S; Mizutani Y; Yakushijin K; Yamashita T; Nakamachi Y; Kawano S; Hayashi Y; Matsuoka H; Minami H
Cytogenet Genome Res; 2016; 149(3):165-170. PubMed ID: 27607436
[TBL] [Abstract][Full Text] [Related]
12. Acute promyelocytic leukemia with complex translocation t(5;17;15)(q35;q21;q22): case report and review of the literature.
Cho SR; Park SJ; Kim HJ; Park IJ; Choi JR; Jung HJ; Park JE
J Pediatr Hematol Oncol; 2011 Oct; 33(7):e326-9. PubMed ID: 21617563
[TBL] [Abstract][Full Text] [Related]
13. Mixed phenotype acute leukemia with t(11;19)(q23;p13.3)/ MLL-MLLT1(ENL), B/T-lymphoid type: A first case report.
Naghashpour M; Lancet J; Moscinski L; Zhang L
Am J Hematol; 2010 Jun; 85(6):451-4. PubMed ID: 20513125
[TBL] [Abstract][Full Text] [Related]
14. CD79a expression in acute myeloid leukemia t(8;21) and the importance of cytogenetics in the diagnosis of leukemias with immunophenotypic ambiguity.
Kozlov I; Beason K; Yu C; Hughson M
Cancer Genet Cytogenet; 2005 Nov; 163(1):62-7. PubMed ID: 16271957
[TBL] [Abstract][Full Text] [Related]
15. Microarray, gene sequencing, and reverse transcriptase-polymerase chain reaction analyses of a cryptic PML-RARA translocation.
Koshy J; Qian YW; Bhagwath G; Willis M; Kelley TW; Papenhausen P
Cancer Genet; 2012 Oct; 205(10):537-40. PubMed ID: 22982005
[TBL] [Abstract][Full Text] [Related]
16. Definition of acute biphenotypic leukemia.
Matutes E; Morilla R; Farahat N; Carbonell F; Swansbury J; Dyer M; Catovsky D
Haematologica; 1997; 82(1):64-6. PubMed ID: 9107085
[TBL] [Abstract][Full Text] [Related]
17. Biphenotypic Acute Leukemia with t(15;17) Lacking Promyelocytic-retinoid Acid Receptor α Rearrangement.
Saito M; Izumiyama K; Mori A; Irie T; Tanaka M; Morioka M; Musashi M
Hematol Rep; 2013; 5(4):e16. PubMed ID: 24416501
[TBL] [Abstract][Full Text] [Related]
18. A pediatric BAL case with double Ph chromosomes and trisomy 5.
Gunden G; Isik S; Ozdemir C; Cİlİngİr O; Bor O; Gokalp EE; Kocagil S; Artan S; Aras BD
Cancer Genet; 2021 Nov; 258-259():7-9. PubMed ID: 34225100
[TBL] [Abstract][Full Text] [Related]
19. Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion.
Tirado CA; Jahn JA; Scheerle J; Eid M; Meister RJ; Christie RJ; Croft CD; Wallingford S; Heritage DW; Mowrey PN; Meloni-Ehrig AM
Cancer Genet Cytogenet; 2005 Aug; 161(1):70-3. PubMed ID: 16080960
[TBL] [Abstract][Full Text] [Related]
20. Detection of minimal residual disease in an AML patient with trisomy 8 using interphase fish.
White DL; Hutchins CJ; Turczynowicz S; Suttle J; Haylock DN; Hughes TP; Juttner CA; To LB
Pathology; 1997 Aug; 29(3):289-93. PubMed ID: 9271020
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
