Novel Philadelphia variant t(Y;9;22)(q12;q34;q11) in a case of chronic myeloid leukemia

Cancer Genetics and Cytogenetics

Volumn 114, Issue 2, 1999, Pages 150-153

  Dierlamm, Judith ^a   Michaux, Lucienne ^b   Stefanova, Margarita ^a   Eggert, Jochen ^c   Leberecht, Petra ^a   Seeger, Doris ^a   Westerhausen, Martin ^c   Hossfeld, Dieter Kurt ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b CLINIQUES UNIVERSITAIRES SAINT LUC   (Belgium)

^c ST JOHANNES HOSPITAL   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROXYUREA;

ADULT; ARTICLE; CASE REPORT; CHROMOSOME YQ; CHRONIC MYELOID LEUKEMIA; COSMID; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FUSION; GENE TRANSLOCATION; HUMAN; MALE; PHILADELPHIA 1 CHROMOSOME; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

ADULT; AGED; BONE MARROW CELLS; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 22; CHROMOSOMES, HUMAN, PAIR 9; FUSION PROTEINS, BCR-ABL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LEUKEMIA, MYELOID, CHRONIC; LEUKEMIA, MYELOID, PHILADELPHIA-POSITIVE; MALE; MIDDLE AGED; PHILADELPHIA CHROMOSOME; VARIATION (GENETICS); Y CHROMOSOME;

EID: 0032869978     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(99)00050-3     Document Type: Article

References (13)

1. Heisterkamp N., Groffen J. Molecular insights into the Philadelphia translocation. Hematol Pathol. 5:1991;1-10.
2. Mitelman F., Heim S. Cancer Cytogenetics. 1995;Wiley-Liss, New York.
3. Dierlamm J., Wlodarska I., Michaux L., La Starza R., Zeller W., Mecucci C., Van den Berghe H. Successful use of the same slide for consecutive fluorescence in situ hybridization (FISH) experiments. Genes Chromosom Cancer. 16:1996;261-264.
4. A complete set of human telomeric probes and their clinical application. Nature Genet. 14:1996;86-89.
5. D'Esposito M., Ciccodicola A., Gianfrancesco F., Esposito T., Flagiello L., Mazzarella R., Schlessinger D., D'Urso M. A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation. Nature Genet. 13:1996;227-229.
6. ISCN (1995): An International System for Human Cytogenetic Nomenclature. F. Mitelman, ed. S. Karger, Basel.
7. Fitzgerald P.H., Morris C.M. Complex chromosomal translocation in the Philadelphia chromosome leukemias. Serial translocations or a concerted genomic rearrangement? Cancer Genet Cytogenet. 57:1991;143-151.
8. Gallego M.S., Baialardo E.M., Gutierrez M., Bonduel M., Feliu A. New variant Ph translocation in chronic myeloid leukemia. t(Y;22)(p11;q11) Cancer Genet Cytogenet. 87:1996;75-78.
9. Sessarego M., Ajmar F., Bianchi Scarra G.L., Ravazzolo R., Boccaccio P. Unusual Ph translocations in CML. four new cases Cancer Genet Cytogenet. 15:1985;199-207.
10. Verhest A., Lustman F. Y-chromosome structural rearrangement in Philadelphia chromosome-negative chronic myelogenous leukemia. N Engl J Med. 303:1980;53-54.
11. Sessarego M., Frassoni F., Defferrari R., Bacigalupo A., Fugazza G., Mareni C., Bruzzone R., Dejana A., Ajmar F. Karyotype evolution of Ph positive chronic myelogenous leukemia patients relapsed in advanced phases of the disease after allogeneic bone marrow transplantation. Cancer Genet Cytogenet. 57:1991;69-78.
12. Blonk M.C., Van der Valk P., Beverstock G.C., Ossenkoppele G.C. Sequential development of peripheral T-cell lymphoma in the course of chronic myelogenous leukemia. Cancer. 66:1990;1198-1203.
13. Cook K.R., Karpen G.H. A rosy future for heterochromatin. Proc Natl Acad Sci USA. 91:1994;5219-5221.