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Items: 1 to 20 of 24

1.

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. doi: 10.1016/j.cancergencyto.2008.03.010.

PMID:
18558291
2.

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 1;144(1):1-5. Review.

PMID:
12810248
3.

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 15;188(2):118-23. doi: 10.1016/j.cancergencyto.2008.09.006. Review.

PMID:
19100517
4.

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. Review.

PMID:
12393282
5.

del(2)(p23) as a sole abnormality in a case of acute myeloid leukemia.

Sundareshan TS, Madhumathi DS, Appaji L.

Cancer Genet Cytogenet. 2002 Apr 15;134(2):172-4. Review.

PMID:
12034535
6.

Deletion of chromosome 6q in two cases of acute myeloblastic leukemia and a review of the literature.

Hirata J, Abe Y, Taguchi F, Takatsuki H, Nishimura J, Nawata H.

Cancer Genet Cytogenet. 1992 Feb;58(2):181-5. Review.

PMID:
1551086
7.

Tetrasomy 21 as a sole chromosome abnormality in acute myeloid leukemia. fluorescence in situ hybridization and spectral karyotyping analyses.

Ohsaka A, Hisa T, Watanabe N, Kojima H, Nagasawa T.

Cancer Genet Cytogenet. 2002 Apr 1;134(1):60-4. Review.

PMID:
11996798
8.

A sole del(15q) anomaly in post-myelodysplasia acute myeloid leukemia.

Yahata N, Ohyashiki K, Iwase O, Kimura Y, Kodama A, Fukutake K, Toyama K.

Leuk Res. 1998 Sep;22(9):845-7. Review.

PMID:
9716017
9.

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. doi: 10.1016/j.cancergencyto.2008.04.011. Review.

PMID:
18656694
10.

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. Review.

PMID:
16584058
11.

A tetraploid minimally differentiated acute myeloblastic leukemia with extensive erythrophagocytosis: a case report and literature review.

Li L, Li J, Li G, Tan Y, Chen X, Ren F, Guo H, Wang H.

Int J Hematol. 2012 Dec;96(6):801-5. doi: 10.1007/s12185-012-1179-6. Review.

PMID:
23054644
12.

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. Review.

PMID:
15064863
13.

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 1;200(1):28-33. doi: 10.1016/j.cancergencyto.2010.03.010. Review.

PMID:
20513531
14.

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 1;196(1):105-8. doi: 10.1016/j.cancergencyto.2009.08.017. Review.

PMID:
19963144
15.

[Pathobiology of acute myeloid leukemia].

Christ O, Feuring-Buske M, Hiddemann W, Buske C.

Med Klin (Munich). 2007 Apr 15;102(4):290-5. Review. German.

PMID:
17426932
16.

A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia.

Park TS, Song J, Lee KA, Lee SG, Yoon S, Kim JS, Lyu CJ, Choi JR.

Cancer Genet Cytogenet. 2007 Dec;179(2):132-5. Review.

PMID:
18036400
17.

Terminal deletion of chromosome 15q26.1: case report and brief literature review.

Bhakta KY, Marlin SJ, Shen JJ, Fernandes CJ.

J Perinatol. 2005 Jun;25(6):429-32. Review.

PMID:
15843813
18.

Acquired acute myelogenous leukemia after therapy for acute promyelocytic leukemia with t(15;17): a case report and review of the literature.

Betancourt-García RD, Castro J, Fernández AC, López-Enríquez A, Fradera J, Pacheco E.

P R Health Sci J. 2009 Jun;28(2):146-50. Review.

PMID:
19530558
19.

Inversion (11)(p15q22) with NUP98-DDX10 fusion gene in pediatric acute myeloid leukemia.

Morerio C, Acquila M, Rapella A, Tassano E, Rosanda C, Panarello C.

Cancer Genet Cytogenet. 2006 Dec;171(2):122-5. Review.

PMID:
17116492
20.

Chronic myelomonocytic leukemia with der(9)t(1;9)(q11;q34) as a sole abnormality.

Suh B, Park TS, Kim JS, Song J, Kim J, Yoo JH, Choi JR.

Ann Clin Lab Sci. 2009 Summer;39(3):307-12. Review.

PMID:
19667417
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