Sequential FISH reveals an abnormal karyotype involving 14 chromosomes in a child with acute lymphoblastic leukemia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Oncology,Cancer Research,Hematology
Link
http://www.nature.com/articles/2401884.pdf
Reference12 articles.
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2. Schrock E, du Manoir S, Veldman T, Schoell B, Weinberg J, Ferguson-Smith MA, Ning Y, Ledbetter DH, Bar-Am I, Soenksen D, Garini Y, Reid T . Multicolor spectral karyotyping of human chromosomes Science 1996 273: 494–497
3. Dierlamm J, Wlodarska I, Michaux L, La Starza R, Zeller W, Mecucci C, Van den Berghe H . Successful use of the same slide for consecutive fluorescence in situ hybridization experiments Genes Chromos Cancer 1996 16: 261–264
4. Chinnappan D, Cowan J, Rastogi A, Miller KB, Blanchard R, Wyandt HE . Discrepant cytogenetic and fluorescence in situ hybridization results in a 26-year-old male with early T-cell acute lymphocytic leukemia Cancer Genet Cytogenet 1998 106: 116–121
5. Berger R, Busson-Le Coniat M . Centric and pericentric chromosome rearrangements in hematopoietic malignancies Leukemia 1999 13: 671–678
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1. Fluorescence In Situ Hybridization (FISH) as a Tool for the Detection of Significant Chromosomal Abnormalities in Childhood Leukaemia;Leukemia;2009
2. Cytogenetics and molecular genetics of acute lymphoblastic leukemia;Reviews in Clinical and Experimental Hematology;2002-06
3. Acute lymphoblastic leukaemia;Best Practice & Research Clinical Haematology;2001-09
4. The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: a valuable resource for patient management;British Journal of Haematology;2001-04
5. The detection and significance of chromosomal abnormalities in childhood acute lymphoblastic leukaemia;Blood Reviews;2001-03
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