These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 12550752)

  • 1. Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myelocytic leukemia.
    Matteucci C; La Starza R; Crescenzi B; Romoli S; Santoro A; Magrin S; Lauria F; Coco FL; Martelli MF; Mecucci C
    Cancer Genet Cytogenet; 2003 Jan; 140(1):13-7. PubMed ID: 12550752
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and molecular cytogenetic studies in ten patients with hematological malignancies characterized by t(20;21)(q11;q11) resulted from del(20q).
    Wu C; Zhang J; Bai S; Yao J; Qiu H; Xue Y; Chen S; Wu Y; Shen J; Pan J
    Cancer Genet; 2016 Oct; 209(10):456-462. PubMed ID: 27810074
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood acute myeloid leukemia. The UK Cancer Cytogenetics Group (UKCCG).
    Jaju RJ; Haas OA; Neat M; Harbott J; Saha V; Boultwood J; Brown JM; Pirc-Danoewinata H; Krings BW; Müller U; Morris SW; Wainscoat JS; Kearney L
    Blood; 1999 Jul; 94(2):773-80. PubMed ID: 10397745
    [TBL] [Abstract][Full Text] [Related]  

  • 4. FISH studies identify the i(20q-) anomaly as a der(20)del(20)(q11q13)idic(20)(p11).
    Li T; Xue Y; Wu Y; Pan J
    Genes Chromosomes Cancer; 2006 Jun; 45(6):536-9. PubMed ID: 16506189
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Clinical and cytogenetic study of 6 cases of hematological disorders associated with 20q- and t (20;21) (q11;q11) abnormalities].
    Wu CX; Pan JL; Qiu HY; Xue YQ; Chen SN; Zhang J; Wu YF; Shen J; Bai SX; Wang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Apr; 30(2):138-42. PubMed ID: 23568721
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Clinical and molecular cytogenetic features of myeloid diseases characterized by i(20q-): a study of seven cases].
    Li TY; Xue YQ; Wu YF; Pan JL; Liu DD; Gong SL
    Zhonghua Yi Xue Za Zhi; 2004 May; 84(9):732-5. PubMed ID: 15200909
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Novel Variant Rearrangement of the Rare Aberration dic(17;20)(p11.2;q11.2) Characterized by Array-CGH as an Insertion in a Patient with Myelodysplastic Syndrome of Multilineage Dysplasia (MDS-MLD).
    Vazmitsel MA; Grammatopoulou V; Yao J; Batanian JR
    Cytogenet Genome Res; 2020; 160(1):22-28. PubMed ID: 32018267
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. New complex t(2;11;17)(p21;q23;q11), a variant form of t(2;11), associated with del(5)(q23q32) in myelodysplastic syndrome-derived acute myeloblastic leukemia.
    Yamamoto K; Nagata K; Morita Y; Inagaki K; Hamaguchi H
    Cancer Genet Cytogenet; 2002 Sep; 137(2):119-23. PubMed ID: 12393282
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deletion (8)(q22) as the only chromosomal abnormality in a patient with RAEB-t with progression to acute myelocytic leukemia.
    Govaerts L; Daenen S; Bong B; Breed A; de Jong B
    Cancer Genet Cytogenet; 1988 Feb; 30(2):319-21. PubMed ID: 3422584
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Isodicentric 20q- in two cases of B-cell acute lymphocytic leukemia with the respective t(9;20)(p11;q11.2) and t(9;22)(q34;q11.2).
    Li T; Xue Y; Zhang J; Chen S; Pan J; Wu Y; Wang Y; Shen J
    Cancer Genet Cytogenet; 2008 Feb; 181(1):55-9. PubMed ID: 18262055
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Isochromosome of a deleted 20q: a rare but recurrent chromosome abnormality in myelodysplastic syndromes.
    Saunders K; Czepulkowski B; Sivalingam R; Hayes JP; Aldouri M; Sekhar M; Cummins M; Ho A; Mufti GJ
    Cancer Genet Cytogenet; 2005 Jan; 156(2):154-7. PubMed ID: 15642396
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignancies.
    MacKinnon RN; Campbell LJ
    Cancer Genet Cytogenet; 2005 Dec; 163(2):176-9. PubMed ID: 16337864
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Myelodysplastic syndrome with translocation (8;21): a distinct myelodysplastic syndrome entity or M2-acute myeloid leukemia with extensive myeloid maturation?
    Kojima K; Omoto E; Hara M; Sasaki K; Katayama Y; Nawa Y; Kimura Y; Azuma T; Takimoto H; Harada M
    Ann Hematol; 1998 Jun; 76(6):279-82. PubMed ID: 9692817
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hidden monosomy 7 in acute myeloid leukemia and myelodysplastic syndrome detected by interphase fluorescence in situ hybridization.
    Arif M; Tanaka K; Damodaran C; Asou H; Kyo T; Dohy H; Kamada N
    Leuk Res; 1996 Sep; 20(9):709-16. PubMed ID: 8947579
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deletion of 16q11 is a recurrent cytogenetic aberration in acute myeloblastic leukemia during disease progression.
    Yamamoto K; Nagata K; Kida A; Hamaguchi H
    Cancer Genet Cytogenet; 2001 Nov; 131(1):65-8. PubMed ID: 11734321
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Complex chromosome translocations of standard t(8;21) and t(15;17) arise from a two-step mechanism as evidenced by fluorescence in situ hybridization analysis.
    Calabrese G; Min T; Stuppia L; Powles R; Swansbury JG; Morizio E; Peila R; Donti E; Fioritoni G; Palka G
    Cancer Genet Cytogenet; 1996 Oct; 91(1):40-5. PubMed ID: 8908165
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dicentric chromosomes and 20q11.2 amplification in MDS/AML with apparent monosomy 20.
    Mackinnon RN; Campbell LJ
    Cytogenet Genome Res; 2007; 119(3-4):211-20. PubMed ID: 18253031
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Two karyotypically unrelated clones with 5q- and 20q- in a primary myelodysplastic syndrome patient evolving into acute nonlymphocytic leukemia.
    Hirokawa M; Miura I; Miura AB
    Int J Hematol; 1995 Aug; 62(2):121-5. PubMed ID: 8590773
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Constitutional t(5;7)(q11;p15) rearranged to acquire monosomy 7q and trisomy 1q in a patient with myelodysplastic syndrome transforming to acute myelocytic leukemia.
    Ganly P; McDonald M; Spearing R; Morris CM
    Cancer Genet Cytogenet; 2004 Mar; 149(2):125-30. PubMed ID: 15036888
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.