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Inv(1)(p22q25) in chronic myeloproliferative disease: constitutional or clonal defect?
1Department of Pathology, Queen Elizabeth Hospital, 30 Gascoigne Road, Hong Kong SAR, China. kfwong@ha.org.hk
Cancer Genetics and Cytogenetics
|March 31, 2005
Abstract:
Pericentric inversion of chromosome 1 is uncommon in chronic myeloproliferative disease. We report the occurrence of an isolated inv(1)(p22q25) in two patients with BCR/ABL-negative chronic myeloproliferative disease. The inv(1) is an acquired clonal abnormality in one patient and a constitutional defect in the other. To our knowledge, this is the first report on the occurrence of inv(1)(p22q25) in hematolymphoid malignancies.
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