The isochromosome (17q) in chronic myelocytic leukaemia: Mechanism of origin, centromeric function and clonal evolution
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00295610.pdf
Reference11 articles.
1. Atkin NB, Amin S, Brito-Babapulle V (1981) Three or four copies of a dicentric 17q isochromosome in an acute myeloproliferative disorder. Cancer Genet Cytogenet 3:75?80
2. Casalone R, Francesconi D, Pasquali F, Comotti B, Vaccari F (1981) Isochromosome (17q) in Philadelphia chromosome (Ph1)-negative juvenile chronic myelocytic leukaemia. Cancer Genet Cytogenet 3:145?148
3. Eiberg H (1974) New selective technique for human chromosomes, Cd staining. Nature 248:55
4. First International Workshop on Chromosomes in Leukaemia (1978) Chromosomes in Ph1-positive chronic granulocytic leukaemia. Br J Haematol 39:305?309
5. Koeffler HP, Golde DW (1981) Chronic myelogenous leukaemia?new concepts (first of two parts). N Engl J Med 304:1201?1209
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2. FISH mapping of i(7q) in acute leukemias and myxoid liposarcoma reveals clustered breakpoints in 7p11.2: implications for formation and pathogenetic outcome of the idic(7)(p11.2);Cytogenetic and Genome Research;2006
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4. Centromere cleavage is a mechanism underlying isochromosome formation in skin and head and neck carcinomas;Chromosoma;2000-11
5. Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course;British Journal of Haematology;1999-08
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