Complex variant t(4;11) characterized by fluorescence in situ hybridization in infant acute lymphoblastic leukemia.

[1]  K. S. Reddy,et al.  A FISH study of variant Philadelphia rearrangements. , 2000, Cancer genetics and cytogenetics.

[2]  L. Chan,et al.  Complex variant 15;17 translocations in acute promyelocytic leukemia. A case report and review of three-way translocations. , 1999, Cancer genetics and cytogenetics.

[3]  D. Arthur,et al.  Cytogenetic studies of infant acute lymphoblastic leukemia: poor prognosis of infants with t(4;11) – a report of the Children’s Cancer Group , 1999, Leukemia.

[4]  A. Smith,et al.  Comparison of metaphase and interphase FISH monitoring of minimal residual disease with MLL gene probe: case study of AML with t(9;11). , 1999, Annales de genetique.

[5]  B. Johansson,et al.  Derivative chromosomes of 11q23-translocations in hematologic malignancies , 1998, Leukemia.

[6]  B. Johansson,et al.  Hematologic malignancies with t(4;11)(q21;q23) – a cytogenetic, morphologic, immunophenotypic and clinical study of 183 cases , 1998, Leukemia.

[7]  D. Nutt,et al.  Case History 3 , 1997 .

[8]  A. Jauch,et al.  Mapping human telomere regions with YAC and P1 clones: chromosome-specific markers for 27 telomeres including 149 STSs and 24 polymorphisms for 14 proterminal regions. , 1996, Genomics.

[9]  M. Bittner,et al.  Chromosome arm painting probes , 1996, Nature Genetics.

[10]  J J Shuster,et al.  Clinical characteristics and treatment outcome of childhood acute lymphoblastic leukemia with the t(4;11)(q21;q23): a collaborative study of 40 cases. , 1991, Blood.

[11]  F. Mitelman,et al.  Catalog of Chromosome Aberrations in Cancer , 1996, British Journal of Cancer.