Spectral karyotyping and multicolor fluorescence in situ hybridization reveal new tumor-specific chromosomal aberrations
Schröck E., Padilla-Nash H. spectral karyotyping and multicolor fluorescence in situ hybridization reveal new tumor-specific chromosomal aberrations. Seminars in Hematology. 37:2000;334-347.
Complex cytogenetic abnormalities in T-lymphoblastic lymphoma: Resolution by spectral karyotyping
Wan T.S.K., Ma S.K., Chan G.C.F., Ching L.M., Ha S.Y., Chan L.C. Complex cytogenetic abnormalities in T-lymphoblastic lymphoma. Resolution by spectral karyotyping Cancer Genet Cytogenet. 118:2000;24-27.
Molecular cytogenetic characterization of acute myeloid leukemia and myelodysplastic syndromes with multiple chromosome rearrangements
Lindvall C., Nordenskiold M., Powit A., Bjorkolm M., Blennow E. Molecular cytogenetic characterization of acute myeloid leukemia and myelodysplastic syndromes with multiple chromosome rearrangements. Haematologica. 86:2001;1158-1164.
Cytogenetic analysis of hematologic malignancies in Hong Kong. A study of 98 cases
Chan L.C., Kwong Y.L., Liu H.W., Todd D., Chan T.K., Ching L.M. Cytogenetic analysis of hematologic malignancies in Hong Kong. A study of 98 cases. Cancer Genet Cytogenet. 62:1992;154-159.
Mitelman database of chromosome aberrations in cancer. Mitelman F, Johnsson B, Mertens F, editor. Available at: http://cgap.nci.gov/Chromosomes/Mitelman. Accessed May 2002.
Atypical chronic myelomonocytic leukemia with eosinophilia and translocation (5;12). A new association
Berkowicz M., Rosner E., Rechavi G., Mamon Z., Neuman Y., Ben-Bassat I., Ramot B. Atypical chronic myelomonocytic leukemia with eosinophilia and translocation (5;12). A new association. Cancer Genet Cytogenet. 51:1991;277-278.
T(5;12)(q31;p21). A clinical entity with features of both myeloid leukemia and chronic myelomonocytic leukemia
Wessels J.W., Fibbe W.E., van der Keur D., Landegent J.E., van der Plas D.C., den Ottolander G.J., Roozendaal K.J., Beverstock G.C. t(5;12)(q31;p21). A clinical entity with features of both myeloid leukemia and chronic myelomonocytic leukemia. Cancer Genet Cytogenet. 65:1993;7-11.
Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation
Golub T.R., Barker G.F., Lovett M., Gilliland D.G. Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell. 77:1994;307-316.
Molecular characterization of der(15)t(11;15) as a secondary cytogenetic abnormality in acute promyelocytic leukemia with cryptic PML-RARα fusion on 17q
Wan T.S.K., Ma S.K., Yip S.F., Yeung Y.M., Chan L.C. Molecular characterization of der(15)t(11;15) as a secondary cytogenetic abnormality in acute promyelocytic leukemia with cryptic PML-RARα fusion on 17q. Cancer Genet Cytogentet. 121:2000;90-93.