BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

213 related articles for article (PubMed ID: 20805702)

  • 21. A rare cytogenetic presentation of acute myeloid leukemia (AML-M2).
    Kumari P; LingappaKavitha B; Obula Reddy C; Mangalagowri M; Madhumathi DS; Mahadeva Prasad M; Raghavendra HV; Premalata CS; Lakshmaiah KC; Mir Mazloumi SH
    Acta Med Iran; 2012; 50(12):827-30. PubMed ID: 23456526
    [TBL] [Abstract][Full Text] [Related]  

  • 22. "Acute myelogenous leukemia like" translocations in CML blast crisis: two new cases of inv(16)/t(16;16) and a review of the literature.
    Patel BB; Mohamed AN; Schiffer CA
    Leuk Res; 2006 Feb; 30(2):225-32. PubMed ID: 16076492
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Coexistent t(8;21)(q22;q22) Translocation and 5q Deletion in Acute Myeloid Leukemia.
    Yamamoto K; Yakushijin K; Sanada Y; Kawamoto S; Matsuoka H; Minami H
    J Clin Exp Hematop; 2015; 55(3):181-5. PubMed ID: 26763368
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Acute myeloid leukemia with t(16;21)(q24;q22) and eosinophilia: case report and review of the literature.
    Park IJ; Park JE; Kim HJ; Jung HJ; Lee WG; Cho SR
    Cancer Genet Cytogenet; 2010 Jan; 196(1):105-8. PubMed ID: 19963144
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Identification of an inversion 16 coexisting with an isochromosome 22q by in situ hybridization in a case of childhood AML M4e.
    Gad SG; Callen DF; Kuss B; Downing JR; Behm F; Head D; Ribeiro RC; Raimondi SC
    Leukemia; 1993 Oct; 7(10):1658-62. PubMed ID: 8412329
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Gain of multiple copies of the CBFB gene: a new genetic aberration in a case of granulocytic sarcoma.
    Mallo M; Espinet B; Salido M; Ferrer A; Pedro C; Besses C; Pérez-Vila E; Serrano S; Florensa L; Solé F
    Cancer Genet Cytogenet; 2007 Nov; 179(1):62-5. PubMed ID: 17981216
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Most Myeloid Neoplasms With Deletion of Chromosome 16q Are Distinct From Acute Myeloid Leukemia With Inv(16)(p13.1q22): A Bone Marrow Pathology Group Multicenter Study.
    Rogers HJ; Hsi ED; Tang G; Wang SA; Bueso-Ramos CE; Lubin D; Morrissette JJ; Bagg A; Cherukuri DP; George TI; Peterson L; Liu YC; Mathew S; Orazi A; Hasserjian RP
    Am J Clin Pathol; 2017 Apr; 147(4):411-419. PubMed ID: 28375434
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Fifty-one patients with acute myeloid leukemia and translocation t(8;21)(q22;q22): an additional deletion in 9q is an adverse prognostic factor.
    Schoch C; Haase D; Haferlach T; Gudat H; Büchner T; Freund M; Link H; Lengfelder E; Wandt H; Sauerland MC; Löffler H; Fonatsch C
    Leukemia; 1996 Aug; 10(8):1288-95. PubMed ID: 8709633
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH.
    Schoch C; Haferlach T; Bursch S; Gerstner D; Schnittger S; Dugas M; Kern W; Löffler H; Hiddemann W
    Genes Chromosomes Cancer; 2002 Sep; 35(1):20-9. PubMed ID: 12203786
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Complex additional chromosomal abnormalities of del(5q), del(7q), and +22 in a patient with acute myelomonocytic leukemia carrying inv(16)].
    Nakaya A; Fujita H; Tachibana T; Takemura S; Ishigatsubo Y
    Rinsho Ketsueki; 2004 Sep; 45(9):1061-3. PubMed ID: 15510837
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Complex translocation (8;12;21): a new variant of t(8;21) in acute myeloid leukemia.
    Farra C; Awwad J; Valent A; Lozach F; Bernheim A
    Cancer Genet Cytogenet; 2004 Dec; 155(2):138-42. PubMed ID: 15571799
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Persistent molecular remission of refractory acute myeloid leukemia with inv(16)(p13.1q22) in an elderly patient induced by cytarabine ocfosfate hydrate.
    Arahata M; Shimizu Y; Asakura H; Nakao S
    J Hematol Oncol; 2015 Feb; 8():5. PubMed ID: 25652695
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Diagnostic value of fluorescence in situ hybridization for the detection of genomic aberrations in older patients with acute myeloid leukemia.
    Fröhling S; Kayser S; Mayer C; Miller S; Wieland C; Skelin S; Schlenk RF; Döhner H; Döhner K;
    Haematologica; 2005 Feb; 90(2):194-9. PubMed ID: 15710571
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Additional chromosomal abnormality of inv(16)(p13q22) to del(7)(q32) in a patient with acute myelomonocytic leukemia].
    Ida T; Hashimoto S; Yano T; Sato N; Koike T
    Rinsho Ketsueki; 2012 Mar; 53(3):347-51. PubMed ID: 22499053
    [TBL] [Abstract][Full Text] [Related]  

  • 35. G-banding and fluorescence in situ hybridization in childhood acute myeloid leukemia from South India.
    Mir Mazloumi SH; Appaji L; Madhumathi DS; Prasannakumari
    Arch Iran Med; 2013 Aug; 16(8):459-62. PubMed ID: 23906250
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Rearrangements of the mixed lineage leukemia gene in acute myeloid leukemia].
    Zhang LJ; Lu XL; He J; Li Y
    Zhonghua Yi Xue Za Zhi; 2006 Aug; 86(32):2256-60. PubMed ID: 17064570
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Patients with t(8;21)(q22;q22) and acute myeloid leukemia have superior failure-free and overall survival when repetitive cycles of high-dose cytarabine are administered.
    Byrd JC; Dodge RK; Carroll A; Baer MR; Edwards C; Stamberg J; Qumsiyeh M; Moore JO; Mayer RJ; Davey F; Schiffer CA; Bloomfield CD
    J Clin Oncol; 1999 Dec; 17(12):3767-75. PubMed ID: 10577848
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Two cases of acute myeloblastic leukemia (M2 type) with karyotypes 45X,-X,t(6;8)(q27;q22),inv(9) and 46,XY,t(8;21)(q22;q22),del(9)(q22).
    Mamaev N; Mamaeva S
    Cancer Genet Cytogenet; 1985 Oct; 18(2):105-11. PubMed ID: 3863694
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Novel chromosome 16 abnormality--der(16)del(16) (q13)t(16;21)(p11.2;q22)--associated with acute myeloid leukemia.
    Sharma P; Watson N; Robson L; Gallo J; Smith A
    Cancer Genet Cytogenet; 1999 Aug; 113(1):25-8. PubMed ID: 10459342
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Incidence of 17p deletions and TP53 mutation in myelodysplastic syndrome and acute myeloid leukemia with 5q deletion.
    Sebaa A; Ades L; Baran-Marzack F; Mozziconacci MJ; Penther D; Dobbelstein S; Stamatoullas A; Récher C; Prebet T; Moulessehoul S; Fenaux P; Eclache V
    Genes Chromosomes Cancer; 2012 Dec; 51(12):1086-92. PubMed ID: 22933333
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.