Translocation (X;20) involving the inactive X chromosome in a patient with myeloproliferative disorder

Cancer Genetics and Cytogenetics

Volumn 158, Issue 1, 2005, Pages 81-83

  O'Reilly, John ^a   Crawford, Julie ^a   Uzaraga, Joan ^b   Cannell, Paul ^a  

^a ROYAL PERTH HOSPITAL   (Australia)

^b KING EDWARD MEMORIAL HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 20; CHROMOSOME 20Q; CHROMOSOME ANALYSIS; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOME REPLICATION; CHROMOSOME TRANSLOCATION X; CHROMOSOME XQ; CYTOGENETICS; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; FEMALE; GENE CLUSTER; GENE FUNCTION; GENETIC ASSOCIATION; GENETIC DISORDER; HUMAN; MYELOPROLIFERATIVE DISORDER; PATIENT; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE; X CHROMOSOME; X CHROMOSOME INACTIVATION;

EID: 14844347288     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2004.08.029     Document Type: Article

References (15)

1. L. Michaux, I. Wlodarska, C. Mecucci, J.M. Hernandez, V. Van Orshoven, J.L. Michaux, and H. Van Den Berghe Characterization by chromosome painting of balanced and unbalanced X chromosome translocations in myelodysplastic syndromes Cancer Genet Cytogenet 82 1995 17 22
2. G.W. Dewald, M. Brecher, L.B. Travis, and P.J. Stupca Twenty-six patients with hematological disorders and X chromosome abnormalities frequent idic(X)(q13) chromosomes and Xq13 anomalies associated with pathologic ringed sideroblasts Cancer Genet Cytogenet 42 1989 173 185
3. B.A. Gray, D. Cornfield, A. Bent-Williams, and R.T. Zori Translocation (X;20)(q13.1;q13.3) as a primary chromosomal finding in two patients with myelocytic disorders Cancer Genet Cytogenet 141 2003 169 174
4. F.A. Asimakopoulos, and A.R. Green Deletions of chromosome 20q and the pathogenesis of myeloproliferative disorders Br J Haematol 95 1996 219 226
5. P.J. Kurtin, G.W. Dewald, D.J. Shields, and C.A. Hanson Hematologic disorders associated with deletions of chromosome 20q: a clinicopathologic study of 107 patients Am J Clin Path 106 1996 680 688
6. M. Aatola, E. Armstrong, L. Teerenhovi, and G.H. Borgstrom Clinical significance of the del(20q) chromosome in hematologic disorders Cancer Genet Cytogenet 62 1992 75 80
7. F. Mitelman ISCN. An international system for human cytogenetic nomenclature 1995 S Karger Basel
8. M.M. Le Beau, C.A. Westbrook, M.O. Diaz, and J.D. Rowley C-src is consistently conserved in the chromosomal deletion (20q) observed in myeloid disorders Proc Natl Acad Sci U S A 82 1985 6692 6696
9. F.A. Asimakopoulos, G.R. Gilbert, M.A. Aldred, T.C. Pearson, and A.R. Green Interstitial deletion constitutes the major mechanism for loss of heterozygosity on chromosome 20q in polycythaemia vera Blood 88 1996 2690 2698
10. D.E. Roulston, R. Espinosa III, M. Stoffel, G.I. Bell, and M.M. Le Beau Molecular genetics of myeloid leukaemia: identification of the commonly deleted segment of chromosome 20 Blood 82 1993 3424 3429
11. A.J. Bench, E.P. Nacheva, T.L. Hood, J.L. Holden, L. French, S. Swanton, K.M. Champion, J. Li, P. Whittaker, G. Stavrides, A.R. Hunt, B.J.P. Huntly, L.J. Campbell, D.R. Bently, P. Deloukas, and A. Green Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes Oncogene 19 2000 3902 3913
12. P. Wang, J.D. Eisenbart, R. Espinosa III, E.M. Davis, R.A. Larson, and M.M. Le Beau Refinement of the smallest deleted segment of chromosome 20 in malignant myeloid diseases and development of a PAC-based physical and transcription map Genomics 67 2000 28 39
13. C. Matteucci, R. La Starza, B. Crescenzi, S. Romoli, A. Santoro, S. Magrin, F. Lauria, F. Lo Coco, M.F. Martelli, and C. Mecucci Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myeloid leukemia Cancer Genet Cytogenet 140 2003 13 17
14. D.L. Van Dyke, W.L. Flejter, M.J. Worsham, J.R. Robertson, J.V. Higgins, H.M. Herr, S. Knuutila, N. Wang, V.R. Babu, and L. Weiss A practical metaphase marker of the inactive X chromosome Am J Hum Genet 39 1986 88 95
15. Z. Gibas, L.M. Gibas, C.A. Filomena, J. Sprandio, and L.G. Jackson Translocation (X;19) with involvement of the inactive X chromosome in oligoblastic granulocytic leukaemia Cancer Genet Cytogenet 35 1988 237 242