BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

286 related articles for article (PubMed ID: 17313849)

  • 1. [Identification of chromosome 21 anomalies in patients with acute myeloid leukemia by fluorescence in situ hybridization].
    Zhang LJ; Wang PP; Lu XL; He J; Li Y; Zhai M
    Zhonghua Yi Xue Za Zhi; 2006 Dec; 86(48):3393-6. PubMed ID: 17313849
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
    Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
    Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. [Abnormalities of chromosome 17 in myeloid malignancies with complex chromosomal abnormalities].
    Zhu Y; Xu W; Liu Q; Pan J; Qiu H; Wang R; Qiao C; Jiang Y; Zhang S; Fan L; Zhang J; Shen Y; Xue Y; Li J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):579-82. PubMed ID: 18841577
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Application of dual-color fluorescence in situ hybridization in acute myeloid leukemia with t (8; 21)].
    Li CW; Bo LJ; Dai Y; Liu XP; Qin S; Liu SH; Wang JX
    Zhonghua Xue Ye Xue Za Zhi; 2006 Jan; 27(1):32-5. PubMed ID: 16732938
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. [Clinical and experimental studies on five cases of acute myeloid leukemia with translocation t(16;21)(p11;q22)].
    Wu Y; Xue Y; Pan J; Ma Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr; 20(2):171-3. PubMed ID: 12673593
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Analysis of complex chromosomal rearrangements in adult patients with MDS and AML by multicolor FISH.
    Babicka L; Ransdorfova S; Brezinova J; Zemanova Z; Sindelarova L; Siskova M; Maaloufova J; Cermak J; Michalova K
    Leuk Res; 2007 Jan; 31(1):39-47. PubMed ID: 16687173
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Screening for NUP98 rearrangements in hematopoietic malignancies by fluorescence in situ hybridization.
    Nebral K; König M; Schmidt HH; Lutz D; Sperr WR; Kalwak K; Brugger S; Dworzak MN; Haas OA; Strehl S
    Haematologica; 2005 Jun; 90(6):746-52. PubMed ID: 15951287
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Two cases of myeloid disorders and a t(8;12) (q12;p13).
    Hernández JM; González MB; García JL; Ferro MT; Gutiérrez NC; Marynen P; San Miguel JF
    Haematologica; 2000 Jan; 85(1):31-4. PubMed ID: 10629588
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular cytogenetic investigations in a novel complex variant of t(8;21)(q22;q22) with ins(15;21)(q15;q22.2q22.3) in a patient with AML-M2 subtype.
    Kokate P; Ahmad F; Dalvi R; Das BR; Mandava S
    Cancer Genet Cytogenet; 2008 Jul; 184(1):52-6. PubMed ID: 18558290
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spectral karyotyping and fluorescence in situ hybridization analyses identified a novel three-way translocation involving inversion 16 in therapy-related acute myeloid leukemia M4eo.
    Ohsaka A; Otsubo K; Yokota H; Hisa T; Saito H; Kozaki T
    Cancer Genet Cytogenet; 2008 Jul; 184(2):113-8. PubMed ID: 18617061
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A clinical and laboratory study of 11 cases of t(6;11)(q27;q23) acute leukemia].
    Pan JL; Xue YQ; Jiang HY; Li TY; Wang Y; Qian J; Wu YF; Wu TQ
    Zhonghua Nei Ke Za Zhi; 2004 Dec; 43(12):920-3. PubMed ID: 15730738
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Systematic screening at diagnosis of -5/del(5)(q31), -7, or chromosome 8 aneuploidy by interphase fluorescence in situ hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: concordances and discrepancies with conventional cytogenetics.
    Beyer V; Castagné C; Mühlematter D; Parlier V; Gmür J; Hess U; Kovacsovics T; Meyer-Monard S; Tichelli A; Tobler A; Jacky E; Schanz U; Bargetzi M; Hagemeijer A; de Witte T; van Melle G; Jotterand M
    Cancer Genet Cytogenet; 2004 Jul; 152(1):29-41. PubMed ID: 15193439
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Detection of aberrant chromosomes in acute lymphoblastic leukemia by fluorescence in situ hybridization].
    Yang K; Huang L
    Zhonghua Xue Ye Xue Za Zhi; 1999 Dec; 20(12):640-2. PubMed ID: 11721367
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q.
    Mrózek K; Heinonen K; Theil KS; Bloomfield CD
    Genes Chromosomes Cancer; 2002 Jun; 34(2):137-53. PubMed ID: 11979548
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cytogenetic study of a patient with infant acute lymphoblastic leukemia using GTG-banding and chromosome painting.
    Alter D; Mark HF
    Exp Mol Pathol; 2000 Oct; 69(2):152-8. PubMed ID: 11001863
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
    Spikes AS; Hegmann K; Smith JL; Shaffer LG
    Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.