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Results: 1 to 20 of 148

1.

Isochromosome 5p and related anomalies: a novel recurrent chromosome abnormality in myeloid disorders.

Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, Guéganic N, Berthou C, De Braekeleer M.

Cancer Genet Cytogenet. 2010 Jul 15;200(2):134-9. doi: 10.1016/j.cancergencyto.2010.04.006.

PMID:
20620596
[PubMed - indexed for MEDLINE]
2.

Gain of an isochromosome 5p: a new recurrent chromosome abnormality in acute monoblastic leukemia.

Schoch C, Bursch S, Kern W, Schnittger S, Hiddemann W, Haferlach T.

Cancer Genet Cytogenet. 2001 May;127(1):85-8.

PMID:
11408074
[PubMed - indexed for MEDLINE]
3.

Gain of an isochromosome 5p: a rare recurrent abnormality in acute myeloid leukemia.

Panani AD.

In Vivo. 2006 May-Jun;20(3):359-60.

PMID:
16724670
[PubMed - indexed for MEDLINE]
Free Article
4.

Multiplex fluorescence in situ hybridization in identifying chromosome involvement of complex karyotypes in de novo myelodysplastic syndromes and acute myeloid leukemia.

Xu W, Li JY, Liu Q, Zhu Y, Pan JL, Qiu HR, Xue YQ.

Int J Lab Hematol. 2010 Feb;32(1 Pt 1):e86-95. doi: 10.1111/j.1751-553X.2008.01101.x. Epub 2008 Oct 13.

PMID:
20089000
[PubMed - indexed for MEDLINE]
5.

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 15;94(2):773-80.

PMID:
10397745
[PubMed - indexed for MEDLINE]
Free Article
6.

The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies.

Maserati E, Pressato B, Valli R, Minelli A, Sainati L, Patitucci F, Marletta C, Mastronuzzi A, Poli F, Lo Curto F, Locatelli F, Danesino C, Pasquali F.

Br J Haematol. 2009 Apr;145(2):190-7. doi: 10.1111/j.1365-2141.2009.07611.x. Epub 2009 Feb 17.

PMID:
19222471
[PubMed - indexed for MEDLINE]
7.

Fluorescence in situ hybridization analysis of 110 hematopoietic disorders with chromosome 5 abnormalities: do de novo and therapy-related myelodysplastic syndrome-acute myeloid leukemia actually differ?

Lessard M, Hélias C, Struski S, Perrusson N, Uettwiller F, Mozziconacci MJ, Lafage-Pochitaloff M, Dastugue N, Terré C, Brizard F, Cornillet-Lefebvre P, Mugneret F, Barin C, Herry A, Luquet I, Desangles F, Michaux L, Verellen-Dumoulin C, Perrot C, Van den Akker J, Lespinasse J, Eclache V, Berger R; Groupe Francophone de Cytogénétique Hématologique.

Cancer Genet Cytogenet. 2007 Jul 1;176(1):1-21.

PMID:
17574959
[PubMed - indexed for MEDLINE]
8.

Redefining monosomy 5 by molecular cytogenetics in 23 patients with MDS/AML.

Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, De Braekeleer M.

Eur J Haematol. 2007 Jun;78(6):457-67. Epub 2007 Mar 28.

PMID:
17391336
[PubMed - indexed for MEDLINE]
9.

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 1;152(1):29-41.

PMID:
15193439
[PubMed - indexed for MEDLINE]
10.

[Detection of common chromosome abnormalities in myelodysplastic syndrome with a panel fluorescence in situ hybridization].

Shen Y, Xue Y, Li J, Pan J, Wu Y, Chen S.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Apr;20(2):160-3. Chinese.

PMID:
12673589
[PubMed - indexed for MEDLINE]
11.
12.

Evaluation of chromosome 5 aberrations in complex karyotypes of patients with myeloid disorders reveals their contribution to dicentric and tricentric chromosomes, resulting in the loss of critical 5q regions.

Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, Morice P, Abgrall JF, Berthou C, De Braekeleer M.

Cancer Genet Cytogenet. 2007 Jun;175(2):125-31.

PMID:
17556068
[PubMed - indexed for MEDLINE]
13.

Several chromosomes involved in translocations with chromosome 5 shown with fluorescence in situ hybridization in patients with malignant myeloid disorders.

Bram S, Rödjer S, Swolin B.

Cancer Genet Cytogenet. 2004 Nov;155(1):74-8.

PMID:
15527906
[PubMed - indexed for MEDLINE]
14.

Is monosomy 5 an uncommon aberration? Fluorescence in situ hybridization reveals translocations and deletions in myelodysplastic syndromes or acute myelocytic leukemia.

Bram S, Swolin B, Rödjer S, Stockelberg D, Ogärd I, Bäck H.

Cancer Genet Cytogenet. 2003 Apr 15;142(2):107-14.

PMID:
12699885
[PubMed - indexed for MEDLINE]
15.

Cytogenetic analysis of de novo acute myeloid leukemia with trilineage myelodysplasia in comparison with myelodysplastic syndrome evolving to acute myeloid leukemia.

Tamura S, Takemoto Y, Hashimoto-Tamaoki T, Mimura K, Sugahara Y, Senoh J, Furuyama JI, Kakishita E.

Int J Oncol. 1998 Jun;12(6):1259-62.

PMID:
9592183
[PubMed - indexed for MEDLINE]
16.

Molecular cytogenetic profiling of complex karyotypes in primary myelodysplastic syndromes and acute myeloid leukemia.

Trost D, Hildebrandt B, Beier M, Müller N, Germing U, Royer-Pokora B.

Cancer Genet Cytogenet. 2006 Feb;165(1):51-63.

PMID:
16490597
[PubMed - indexed for MEDLINE]
17.
18.

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 15;156(2):154-7.

PMID:
15642396
[PubMed - indexed for MEDLINE]
19.

Conventional and molecular cytogenetic features of myelodysplastic syndrome in China.

Chen L, Li J, Zhu Y, Qiu H, Pan J, Wang R, Qian S, Xu W, Xue Y.

Exp Oncol. 2007 Dec;29(4):299-303.

PMID:
18199987
[PubMed - indexed for MEDLINE]
20.

[Detection of cytogenetic abnormalities involving chromosomes 5,7 and 8 in myelodysplastic syndromes with fluorescence in situ hybridization and its clinical significance].

Cai Y, Qin YW, Wang C, Yang J, Yan SK.

Zhonghua Xue Ye Xue Za Zhi. 2007 Jan;28(1):6-10. Chinese.

PMID:
17649717
[PubMed - indexed for MEDLINE]

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