37 related articles for article (PubMed ID: 18558291)
1. Deletion of chromosome arm 15q and hitherto unreported duplication of del(15q) in myeloid disorders.
Saunders K; Williams Y; Aldouri M; Telford N; Czepulkowski B
Cancer Genet Cytogenet; 2004 Jun; 151(2):146-51. PubMed ID: 15172752
[TBL] [Abstract][Full Text] [Related]
2. A novel subtelomeric translocation t(5;9) and a deletion of the RB1 gene in a patient with acute myeloid leukemia (AML-M0).
Lee J; Lu X; Shin ES; Kern WF; Mulvihill JJ; Li S
Cancer Genet Cytogenet; 2008 Feb; 181(1):36-9. PubMed ID: 18262051
[TBL] [Abstract][Full Text] [Related]
3. del(6)(p23) in two cases of de novo AML--a new recurrent primary chromosome abnormality.
Anwar Iqbal M; Al-Omar HM; Owaidah T; Al-Humaidan H; Bhuiyan ZA; Sahovic E
Eur J Haematol; 2006 Sep; 77(3):245-50. PubMed ID: 16856925
[TBL] [Abstract][Full Text] [Related]
4. A cryptic deletion in 5q31.2 provides further evidence for a minimally deleted region in myelodysplastic syndromes.
MacKinnon RN; Kannourakis G; Wall M; Campbell LJ
Cancer Genet; 2011 Apr; 204(4):187-94. PubMed ID: 21536236
[TBL] [Abstract][Full Text] [Related]
5. Deletion of chromosome arm 15q in a case of minimally differentiated hypoplastic AML-M0.
Fujieda A; Masuya M; Kitano S; Miyazaki K; Yazaki A; Sugimoto Y; Usui E; Miyata E; Shibasaki T; Yamamura K; Ohishi K; Nishii K; Nakase K; Takeuchi T; Katayama N
Cancer Genet Cytogenet; 2008 Jul; 184(1):57-61. PubMed ID: 18558291
[TBL] [Abstract][Full Text] [Related]
6. Deletion 15q as the sole abnormality in acute myeloid leukemia: report of three cases and review of the literature.
Lu G; Yin CC; Medeiros LJ; Abruzzo LV
Cancer Genet Cytogenet; 2009 Jan; 188(2):118-23. PubMed ID: 19100517
[TBL] [Abstract][Full Text] [Related]
7. Deletion of chromosome 15 represents a rare but recurrent chromosomal abnormality in myelocytic malignancies.
Dierlamm J; Schilling G; Michaux L; Hinz K; Murga Penas EM; Seeger D; Hagemeijer A; Hossfeld DK
Cancer Genet Cytogenet; 2003 Jul; 144(1):1-5. PubMed ID: 12810248
[TBL] [Abstract][Full Text] [Related]
8. RUNX1-MTG16 fusion gene in acute myeloblastic leukemia with t(16;21)(q24;q22): case report and review of the literature.
De Braekeleer E; Douet-Guilbert N; Le Bris MJ; Morel F; Férec C; De Braekeleer M
Cancer Genet Cytogenet; 2008 Aug; 185(1):47-50. PubMed ID: 18656694
[TBL] [Abstract][Full Text] [Related]
9. Identification of the translocation t(15;17) in acute myeloid leukemia (AML) initially classified as FAB M1: case report and review of the literature.
Braham Jmili N; Omri H; Senana Sendi H; Fekih S; Hizem S; Sriha B; Khelif A; Saad A; Kortas M
Clin Lab; 2006; 52(3-4):125-30. PubMed ID: 16584058
[TBL] [Abstract][Full Text] [Related]
10. Deletion (11)(q13) as the sole anomaly in myeloid malignancies: four new cases and a short review.
Panani AD; Pappa V; Papageorgiou S; Stamatelli F; Raptis SA
Ann Hematol; 2004 Mar; 83(3):153-5. PubMed ID: 15064863
[TBL] [Abstract][Full Text] [Related]
11. Essential thrombocythemia with myelofibrosis transformed into acute myeloid leukemia with der(1;15)(q10;q10): case report and literature review.
Charafeddine KM; Mahfouz RA; Zaatari GS; Ibrahim GY; Muwakkit SA; Najm ND; Farra CG
Cancer Genet Cytogenet; 2010 Jul; 200(1):28-33. PubMed ID: 20513531
[TBL] [Abstract][Full Text] [Related]
12.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
13.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
