Dicentric (1;15) in myeloid disorders

Cancer Genetics and Cytogenetics

Volumn 88, Issue 1, 1996, Pages 86-89

  Michaux, Lucienne ^a   Dierlamm, Judith ^a   Mecucci, Cristina ^a,c   Meeus, Peter ^a   Ameye, Geneviève ^b   Libouton, Jeanne Marie ^b   Verhoef, Gregor ^a   Ferrant, Augustin ^b   Louwagie, Andries ^b   Verellen Dumoulin, Christine ^b   Van Den Berghe, Herman ^a,d  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b Department of Hematology ^*

^c UNIVERSITY OF PERUGIA   (Italy)

^d CENTER FOR HUMAN GENETICS   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; BLOOD CELL COUNT; BONE MARROW BIOPSY; BONE MARROW TRANSPLANTATION; CHROMOSOME 1; CHROMOSOME 15; CHROMOSOME ANALYSIS; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; DICENTRIC CHROMOSOME; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MACROCYTIC ANEMIA; MALE; MYELODYSPLASTIC SYNDROME; POLYCYTHEMIA VERA; PRIORITY JOURNAL;

EID: 0029898246     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/0165-4608(95)00218-9     Document Type: Article

References (10)

1. Bennett J, Catovsky D, Daniel MT, Flandrin G, Galton D, Gralnick H, Sultan C (1982): Proposals for the classification of the myelodysplastic syndromes. Br J Haematol 51:189-199.
2. Mecucci C, Tricot G, Boogaerts M, Van Den Berghe H (1986): An identical translocation between chromosome 1 and 15 in two patients with myelodysplastic syndromes. Br J Haematol 62:439-445.
3. Mascarello JT, Osborn C, Kadota RP (1989): A dysmorphic child with myelodysplasia characterized by a duplication of 1q and multiple duplications of 3q. Cancer Genet Cytogenet 38:9-12.
4. Jotterand-Bellomo M, Parlier V, Schmidt PM, Beris P (1990): Cytogenetic analysis of 54 cases of myelodysplastic syndrome. Cancer Genet Cytogenet 46:157-172.
5. Wurster-Hill D, Whang-Peng J, McIntyre R, Hsu LYF, Hirschhorn K, Modan B, Pisciotta AV, Pierre R, Balcerzak SP, Weinfeld A, Murphy S (1976): Cytogenetic studies in polycythemia vera. Semin Hematol 13:13-32.
6. Swolin B, Weinfeld A, Westin J (1986): Trisomy 1q in polycythemia vera and its relation to disease transition. Am J Hematol 22:155-167.
7. ISCN (1991): Guideline for Cancer Cytogenetics, Supplement to An International System for Human Cytogenetic Nomenclature, F Mitelmen, ed. Karger, Basel, 1991.
8. Lichter P, Boyle AL, Cremer T, Ward DC (1991): Analysis of genes and chromosomes by nonisotopic in situ hybridisation. GATA 8:25-35.
9. Fonatsch C, Haase D, Freund M, Bartels H, Tesch M (1991): Partial trisomy 1q. A nonrandom primary chromosomal abnormality in myelodysplastic syndromes? Cancer Genet Cytogenet 56:243-253.
10. Cook KR, Karpen GH (1994): A rosy future for heterochromatin. Proc Natl Acad Sci USA 91:5219-5221.