The Philadelphia chromosome as a secondary abnormality in two cases of acute myeloid leukemia-Reference-Cited by-同舟云学术

The Philadelphia chromosome as a secondary abnormality in two cases of acute myeloid leukemia

Published:1998-08 Issue:3 Volume:102 Page:873-875
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:British Journal of Haematology

Author:

Mozziconacci Marie-Joëlle,Sainty Danielle,Gabert Jean,Arnoulet Christine,Simonetti Jacqueline,Toiron Yves,Costello Régis,Hagemeijer Anne,Lafage-Pochitaloff Marina

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.1998.0887b.x/fullpdf

Reference7 articles.

1. t(15;17) in a promyelocytic form of chronic myeloid leukemia blastic crisis;Berger;Cancer Genetics and Cytogenetics,1983

2. Chromosome 3q21 abnormalities associated with hyperactive thrombopoiesis in acute blastic transformation of chronic myeloid leukemia;Bernstein;Blood,1986

3. Detection of major bcr-abl gene expression at a very low level in blood cells of some healthy individuals;Biernaux;Blood,1995

4. Association of t(15;17) and t(8;21) in the initial phase of an acute promyelocytic leukemia;Charrin;Cancer Genetics and Cytogenetics,1992

5. The Philadelphia chromosome as a secondary change in leukemia: three case reports and an overview of the literature;Chen;Cancer Genetics and Cytogenetics,1998

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