Morphology, cytogenetics, and survival in myelodysplasia with del(20q) or ider(20q): a multicenter study-Reference-Cited by-同舟云学术

Morphology, cytogenetics, and survival in myelodysplasia with del(20q) or ider(20q): a multicenter study

Published:2011-07-09 Issue:2 Volume:91 Page:203-213
ISSN:0939-5555
Container-title:Annals of Hematology
language:en
Short-container-title:Ann Hematol

Author:

Mullier François,Daliphard Sylvie,Garand Richard,Dekeyser Mélanie,Cornet Yvan,Luquet Isabelle,Talmant Pascaline,Richebourg Steven,Jamar Mauricette,Dogné Jean-Michel,Chatelain Christian,Michaux Lucienne,Chatelain Bernard

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00277-011-1286-0.pdf

Reference39 articles.

1. 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(3):337–342

2. Douet-Guilbert N, Lai JL, Basinko A, Gueganic N, Andrieux J, Pollet B, Plantier I, Delattre C, Crepin O, Corm S, Le Bris MJ, Morel F, De Braekeleer M (2008) Fluorescence in situ hybridization characterization of ider(20q) in myelodysplastic syndrome. Br J Haematol 143(5):716–720

3. Ligon AH, DeAngelo DJ, Atkins L, Dal Cin P (2005) Isochromosome of a deleted 20q may be a relatively common abnormality in myeloid malignancies. Cancer Genet Cytogenet 162(1):89–91

4. MacKinnon RN, Campbell LJ (2005) 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. Cancer Genet Cytogenet 163(2):176–179

5. Saunders K, Czepulkowski B, Sivalingam R, Hayes JP, 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(2):154–157

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