The incidences of trisomy 8, trisomy 9 and D20S108 deletion in polycythaemia vera: an analysis of blood granulocytes using interphase fluorescence in situ hybridization-Reference-Cited by-同舟云学术

The incidences of trisomy 8, trisomy 9 and D20S108 deletion in polycythaemia vera: an analysis of blood granulocytes using interphase fluorescence in situ hybridization

Published:2000-09 Issue:4 Volume:110 Page:839-846
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:

Author:

Westwood N. B.,Gruszka-Westwood A. M.,Pearson C. E.,DeLord C. F. M.,Green A. R.,Huntly B. J. P.,Lakhani A.,McMullin M. F.,Pearson T. C.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2000.02242.x/fullpdf

Reference28 articles.

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2. Interstitial deletion constitutes the major mechanism for loss of heterozygosity on chromosome 20q in polycythemia vera;Asimakopoulos;Blood,1996a

3. Detection of chromosome 20q deletions in bone marrow metaphases but not peripheral blood granulocytes in patients with myeloproliferative disorders or myelodysplastic syndromes;Asimakopoulos;Blood,1996b

4. Molecular genetics and cytogenetics of myeloproliferative disorders;Bench;Baillieres Clinical Haematology,1998

5. Clonality in myeloproliferative disorders;Blanchard;American Journal of the Medical Sciences,1992

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