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Proceedings of the National Academy of Sciences of the United States of America|March 1, 1986
Heterogeneity of chromosome 22 breakpoint in Philadelphia-positive (Ph+) acute lymphocytic leukemiaJ Erikson, C A Griffin, A ar-Rushdi, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1984
A human c-erbA oncogene homologue is closely proximal to the chromosome 17 breakpoint in acute promyelocytic leukemiaA I Dayton, J R Selden, G Laws, et al.
Journal of Pediatric Hematology/Oncology|August 14, 1998
MLL genomic breakpoint distribution within the breakpoint cluster region in de novo leukemia in childrenC A Felix, M R Hosler, D J Slater, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 2000
Panhandle PCR for cDNA: a rapid method for isolation of MLL fusion transcripts involving unknown partner genesM D Megonigal, E F Rappaport, R B Wilson, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 9, 2001
Near-precise interchromosomal recombination and functional DNA topoisomerase II cleavage sites at MLL and AF-4 genomic breakpoints in treatment-related acute lymphoblastic leukemia with t(4;11) translocationB D Lovett, L Lo Nigro, E F Rappaport, et al.
The British Journal of Dermatology|September 21, 2004
BCL2 and JUNB abnormalities in primary cutaneous lymphomasX Mao, G Orchard, D M Lillington, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Association of CYP3A4 genotype with treatment-related leukemiaC A Felix, A H Walker, B J Lange, et al.
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