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Methods in Molecular Biology (Clifton, N.J.)|March 12, 2009
Specialized fluorescence in situ hybridization (FISH) techniques for leukaemia researchLyndal Kearney, Sue ColmanMethods in Molecular Biology (Clifton, N.J.)|June 8, 2012
Fluorescence in situ hybridization for cancer-related studiesLyndal Kearney, Janet ShipleyChromosoma|July 9, 2005
Molecular cytogenetics in haematological malignancy: current technology and future prospectsLyndal Kearney, Sharon W HorsleyGenes, Chromosomes & Cancer|May 12, 2006
MLL chimeric protein activation renders cells vulnerable to chromosomal damage: an explanation for the very short latency of infant leukemiaMariko Eguchi, Minenori Eguchi-Ishimae, Deborah Knight, et al.Genes, Chromosomes & Cancer|March 9, 2006
Array CGH of fusion gene-positive leukemia-derived cell lines reveals cryptic regions of genomic gain and lossSharon W Horsley, Alan Mackay, Marjan Iravani, et al.Genes, Chromosomes & Cancer|June 12, 2003
Prenatal chromosomal diversification of leukemia in monozygotic twinsHelena Kempski, Karen A Mensa-Bonsu, Lyndal Kearney, et al.Blood|March 16, 2002
A cryptic t(5;11)(q35;p15.5) in 2 children with acute myeloid leukemia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assayJill Brown, Mays Jawad, Stephen R F Twigg, et al.Genes, Chromosomes & Cancer|January 9, 2008
Genetic lesions in a preleukemic aplasia phase in a child with acute lymphoblastic leukemiaSharon W Horsley, Susan Colman, Mark McKinley, et al.Genome Research|September 24, 2013
Single-cell mutational profiling and clonal phylogeny in cancerNicola E Potter, Luca Ermini, Elli Papaemmanuil, et al.Genes, Chromosomes & Cancer|August 27, 2003
Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemiaSabrina Tosi, Jim Hughes, Stephen W Scherer, et al.Pageof 3