No increased frequency of trisomies 8 and 9 by fluorescence in situ hybridization in untreated patients with essential thrombocythemia-Reference-Cited by-同舟云学术

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No increased frequency of trisomies 8 and 9 by fluorescence in situ hybridization in untreated patients with essential thrombocythemia

Published:2001-04 Issue:1 Volume:126 Page:56-59
ISSN:0165-4608
Container-title:Cancer Genetics and Cytogenetics
language:en
Short-container-title:Cancer Genetics and Cytogenetics

Author:

Swolin Birgitta,Safai-Kutti Soodabeh,Anghem Eva,Kutti Jack

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference17 articles.

1. The management of thrombocytosis;Kutti;Eur J Haematol,1990

2. Primary thrombocytosis;Pearson;Br J Haematol,1991

3. Experience of the Polycythemia Vera Study Group with essential thrombocythemia;Murphy;Semin Hematol,1997

4. Cancer cytogenetics. Chromosomal and molecular genetic aberrations of tumor cells,1995

5. Chromosome studies in untreated polycythemia vera;Westin;Scand J Haematol,1976

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1. Portal Hypertension and Myeloproliferative Neoplasms: A Relationship Revealed;ISRN Hematology;2013-09-16

2. Molecular Pathogenesis of Nonchronic Myeloid Leukemia Myeloproliferative Neoplasms;Molecular Pathology Library;2010

3. Cytogenetic abnormalities in essential thrombocythemia: prevalence and prognostic significance;European Journal of Haematology;2009-07

4. Pathogenetic insight and prognostic information from standard and molecular cytogenetic studies in the BCR-ABL-negative myeloproliferative neoplasms (MPNs);Leukemia;2008-08-28

5. Cytogenetic and molecular aspects of Philadelphia negative chronic myeloproliferative disorders: Clinical implications;Cancer Letters;2007-09

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