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Isochromosome 17q in two cases of acute blast transformation in myeloproliferative disorders.

作者信息

McDermott A, Romain D, Fraser I D, Scott G L

出版信息

Hum Genet. 1978 Dec 18;45(2):215-8. doi: 10.1007/BF00286966.

DOI:10.1007/BF00286966
PMID:738722
Abstract

Two cases of acute blast cell transformation in myeloproliferative disorders associated with a dicentric 17q isochromosome are reported. In both cases, the karyotypes also included a Philadelphia 9q;22q translocation, and in one case, an additional chromosome 8 (trisomy 8).

摘要

相似文献

1
Isochromosome 17q in two cases of acute blast transformation in myeloproliferative disorders.
Hum Genet. 1978 Dec 18;45(2):215-8. doi: 10.1007/BF00286966.
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引用本文的文献

1
The isochromosome (17q) in chronic myelocytic leukaemia: mechanism of origin, centromeric function and clonal evolution.
Hum Genet. 1982;62(1):89-90. doi: 10.1007/BF00295610.

本文引用的文献

1
Marrow chromosome studies in "preleukemia". Further correlation with clinical course.“白血病前期”的骨髓染色体研究。与临床病程的进一步相关性。
Cancer. 1971 Aug;28(2):513-8. doi: 10.1002/1097-0142(197108)28:2<513::aid-cncr2820280233>3.0.co;2-0.
2
Editorial: The role of cytogenetics in hematology.社论：细胞遗传学在血液学中的作用。
Blood. 1976 Jul;48(1):1-7.
3
The cytogenetics of chronic granulocytic leukaemia.
Clin Haematol. 1977 Feb;6(1):55-75.