Isoderivative of deleted chromosome 20 in primary myelofibrosis (PMF) characterized by molecular cytogenetics and array CGH-Reference-Cited by-同舟云学术

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Isoderivative of deleted chromosome 20 in primary myelofibrosis (PMF) characterized by molecular cytogenetics and array CGH

Published:2009-05-15 Issue:11 Volume:88 Page:1157-1159
ISSN:0939-5555
Container-title:Annals of Hematology
language:en
Short-container-title:Ann Hematol

Author:

Douet-Guilbert N.,Andrieux J.,Laï J. L.,Morice P.,Demory J. L.,Basinko A.,Ugo V.,Gueganic N.,Le Bris M. J.,Morel F.,De Braekeleer M.

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00277-009-0753-3.pdf

Reference8 articles.

1. GFCH (2004) Recommandations pour la prise en charge cytogénétique des syndromes myéloprolifératifs autres que la leucémie myéloïde chronique (LMC) établies par le Groupe Français de Cytogénétique Hématologique (GFCH). Pathol Biol 52:241–244. doi: 10.1016/j.patbio.2004.04.003

2. Li T, Xue Y, Wu Y, Pan J (2004) Clinical and molecular cytogenetic studies in seven patients with myeloid diseases characterized by i(20q-). Br J Haematol 125:337–342. doi: 10.1111/j.1365-2141.2004.04921.x

3. Saunders K, Czepulkowski B, Sivalingam R, Hayes JPLA, Aldouri M, Sekhar M, Cummins M, Ho A, Mufti GJ (2005) Isochromosome of a deleted 20q: a rare but recurrent chromosome abnormality in myelodysplastic syndromes. Cancer Genet Cytogenet 156:154–157. doi: 10.1016/j.cancergencyto.2004.03.018

4. Lim TH, Lim AS, Tien SL (2006) A novel isoderivative chromosome 20 in a patient with chronic myelomonocytic leukemia. Cancer Genet Cytogenet 170:80–82. doi: 10.1016/j.cancergencyto.2006.04.005

5. Shetty S, Roland B (2008) Isoderivative chromosome 20 in bone marrow: three new cases. Cancer Genet Cytogenet 184:72–73. doi: 10.1016/j.cancergencyto.2008.03.003

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Fusion of the additional sex combs like 1 and teashirt zinc finger homeobox 2 genes resulting from ider(20q) aberration in a patient with myelodysplastic syndrome;British Journal of Haematology;2013-10-10

2. L’association des neutrophiles hypogranulaires et vacuolisés à l’érythrophagocytose par les neutrophiles est un marqueur utile dans les syndromes myélodysplasiques avec del(20q) ou ider(20q) : une étude multicentrique;Immuno-analyse & Biologie Spécialisée;2012-02

3. Morphology, cytogenetics, and survival in myelodysplasia with del(20q) or ider(20q): a multicenter study;Annals of Hematology;2011-07-09

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