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381 related items for PubMed ID: 20226962

  • 1. 8p11 myeloproliferative syndrome: a review.
    Jackson CC, Medeiros LJ, Miranda RN.
    Hum Pathol; 2010 Apr; 41(4):461-76. PubMed ID: 20226962
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  • 2. Molecular monitoring of 8p11 myeloproliferative syndrome in an infant.
    Zhang WW, Habeebu S, Sheehan AM, Naeem R, Hernandez VS, Dreyer ZE, López-Terrada D.
    J Pediatr Hematol Oncol; 2009 Nov; 31(11):879-83. PubMed ID: 19829149
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  • 8. [Clinical pathological features of the 8p11 myeloproliferative syndrome].
    Yan Z, Yang B, Wang QS, Wang LL, Han XP, Ren F, Yu L.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2010 Oct; 18(5):1321-6. PubMed ID: 21129285
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  • 10. Identification of a novel partner gene, TPR, fused to FGFR1 in 8p11 myeloproliferative syndrome.
    Li F, Zhai YP, Tang YM, Wang LP, Wan PJ.
    Genes Chromosomes Cancer; 2012 Sep; 51(9):890-7. PubMed ID: 22619110
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  • 11. t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12.
    Chaffanet M, Popovici C, Leroux D, Jacrot M, Adélaïde J, Dastugue N, Grégoire MJ, Hagemeijer A, Lafage-Pochitaloff M, Birnbaum D, Pébusque MJ.
    Oncogene; 1998 Feb 19; 16(7):945-9. PubMed ID: 9484786
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  • 12. Biphenotypic hematologic malignancy: a case report of the 8p11 myeloproliferative syndrome in a child.
    Chen X, Zhang Y, Li Y, Lei P, Zhai Y, Liu L.
    J Pediatr Hematol Oncol; 2010 Aug 19; 32(6):501-3. PubMed ID: 20562652
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  • 14. Myeloproliferative neoplasms with t(8;22)(p11.2;q11.2)/BCR-FGFR1: a meta-analysis of 20 cases shows cytogenetic progression with B-lymphoid blast phase.
    Montenegro-Garreaud X, Miranda RN, Reynolds A, Tang G, Wang SA, Yabe M, Wang W, Fang L, Bueso-Ramos CE, Lin P, Medeiros LJ, Lu X.
    Hum Pathol; 2017 Jul 19; 65():147-156. PubMed ID: 28551329
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  • 15. t(8;13)-positive bilineal lymphomas: report of 6 cases.
    Vega F, Medeiros LJ, Davuluri R, Cromwell CC, Alkan S, Abruzzo LV.
    Am J Surg Pathol; 2008 Jan 19; 32(1):14-20. PubMed ID: 18162765
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  • 16. Combined translocation with ZNF198-FGFR1 gene fusion and deletion of potential tumor suppressors in a myeloproliferative disorder.
    Etienne A, Gelsi-Boyer V, Carbuccia N, Adélaïde J, Barba G, La Starza R, Murati A, Eclache V, Birg F, Birnbaum D, Mozziconacci MJ, Mecucci C, Chaffanet M.
    Cancer Genet Cytogenet; 2007 Mar 19; 173(2):154-8. PubMed ID: 17321332
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  • 17. 8p11 myeloproliferative syndrome: diagnostic challenges and pitfalls.
    Antic DA, Vukovic VM, Milosevic Feenstra JD, Kralovics R, Bogdanovic AD, Dencic Fekete MS, Mihaljevic BS.
    J BUON; 2016 Mar 19; 21(3):745-9. PubMed ID: 27569099
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  • 18. Identification of a novel gene, FGFR1OP2, fused to FGFR1 in 8p11 myeloproliferative syndrome.
    Grand EK, Grand FH, Chase AJ, Ross FM, Corcoran MM, Oscier DG, Cross NC.
    Genes Chromosomes Cancer; 2004 May 19; 40(1):78-83. PubMed ID: 15034873
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  • 19. 8p11 myeloproliferative syndrome preceded by t(8;9)(p11;q33), CEP110/FGFR1 fusion transcript: morphologic, molecular, and cytogenetic characterization of myeloid neoplasms associated with eosinophilia and FGFR1 abnormality.
    Park TS, Song J, Kim JS, Yang WI, Song S, Kim SJ, Suh B, Choi JR.
    Cancer Genet Cytogenet; 2008 Mar 19; 181(2):93-9. PubMed ID: 18295660
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  • 20. Favorable outcome of allogeneic hematopoietic cell transplantation for 8p11 myeloproliferative syndrome associated with BCR-FGFR1 gene fusion.
    Dolan M, Cioc A, Cross NC, Neglia JP, Tolar J.
    Pediatr Blood Cancer; 2012 Jul 15; 59(1):194-6. PubMed ID: 22106025
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