Complex cytogenetic abnormalities in T-lymphoblastic lymphoma: Resolution by spectral karyotyping

Cancer Genetics and Cytogenetics

Volumn 118, Issue 1, 2000, Pages 24-27

  Wan, T S K ^a   Ma, S K ^a   Chan, G C F ^a   Ching, L M ^a   Ha, S Y ^a   Chan, L C ^a  

^a UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CHROMOSOME 13Q; CHROMOSOME 16Q; CHROMOSOME 18; CHROMOSOME 1P; CHROMOSOME 2Q; CHROMOSOME 5; CHROMOSOME 5Q; CHROMOSOME 7P; CHROMOSOME 7Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION; CHROMOSOME TRANSLOCATION 2; CHROMOSOME TRANSLOCATION 4; CYTOGENETICS; HUMAN; HUMAN CELL; KARYOTYPING; LYMPH NODE; LYMPHOBLASTOMA; MALE; PRIORITY JOURNAL; T LYMPHOBLAST; TECHNIQUE;

EID: 0034175958     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(99)00174-0     Document Type: Article

References (11)

1. Goldsby R.E., Carroll W.L. The molecular biology of pediatric lymphomas. J Pediatr Hematol Oncol. 20:1998;282-296.
2. Offit K., Jhanwar S.C., Ladanyi M., Filippa D.A., Chaganti R.S.K. Cytogenetic analysis of 434 consecutively ascertained specimens of non-Hodgkin's lymphoma. correlation between recurrent aberrations, histology, and exposure to cytotoxic treatment Genes Chromosom Cancer. 3:1991;189-201.
3. th Ed:1994;Wiley-Liss, New York.
4. Harris N.L., Jaffe E.S., Stein H., Banks P.M., Chan J.K.C., Cleary M.L., Delsol G., De Wolf-Peeters C., Falini B., Gatter K.C., Grogan T.M., Isaacson P.G., Knowles D.M., Mason D.Y., Muller-Hermelink H.-K., Pileri S.A., Piris M.A., Ralfkiaer E., Warnke R.A. A revised European-American classification of lymphoid neoplasms. a proposal from the International Lymphoma Study Group Blood. 84:1994;1361-1392.
5. Chan L.C., Ha S.Y., Ching L.M., Lee C.P., Lau Y.L., Yeun P., Leung N.K. Cytogenetics and immunophenotypes of childhood acute lymphoblastic leukemia in Hong Kong. Cancer Genet Cytogenet. 76:1994;118-124.
6. ISCN (1995): An International System for Human Cytogenetic Nomenclature. F Mitelman, ed. S. Karger, Basel.
7. Schröck E., du Manoir S., Veldman T., Schoell B., Wienberg J., Ferguson-Smith M.A., Ning Y., Ledbetter D.H., Bar-AM I., Soenksen D., Garini Y., Ried T. Multicolor spectral karyotyping of human chromosomes. Science. 273:1996;494-497.
8. Rothmann C., Bar-Am I., Malik Z. Spectral imaging for quantitative histology and cytogenetics. Histol Histopathol. 13:1998;921-926.
9. Veldman T., Vignon C., Schröck E., Rowley J.D., Ried T. Hidden chromosome abnormalities in hematological malignancies detected by multicolor spectral karyotyping. Nature Genet. 15:1997;406-410.
10. Bajalica S., Sørensen A.-G., Tingaard Pedersen N., Heim S., Brondum-Nielsen K. Chromosome painting as a supplement to cytogenetic banding analysis in non-Hodgkin's lymphoma. Genes Chromosom Cancer. 7:1993;231-239.
11. Jaju R.J., Haas O.A., Neat M., Harbott J., Boultwood J., Saha V., Krings B.W., Müller U., Morris S.W., Wainscoat J.S., Kearny L. A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5p) in childhood AML. Blood. 92(suppl 1):1998;311a.