t(X;17) as the sole karyotypic anomaly in a case of M3r subtype of acute promyelocytic leukemia without RARα rearrangement

Author:

Wang Huan-Ping,Xu Huan,Chen Zhi-Mei,Tong Xiang-Min,Qian Wen-Bin,Jin Jie

Publisher

Elsevier BV

Subject

Cancer Research,Oncology,Hematology

Reference7 articles.

1. A new morphologic classification system for acute promyelocytic leukemia distinguishes cases with underlying PLZF/RARα gene rearrangements;Sainty;Blood,2000

2. Complex variant 15;17 translocations in acute promyelocytic leukemia. A case report and review of three-way translocations;Wan;Cancer Genet Cytogenet,1999

3. A variant t(X;15)(p11;q22) translocation in acute promyelocytic leukemia;Srivastava;Cancer Genet Cytogenet,1987

4. Han Y, Xue Y, Zhang J, Pan J, Wu Y, Bai S. Y-Chromosome loss as the sole karyotypic anomaly with 3′RARα submicroscopic deletion in a case of M3r subtype of acute promyelocytic leukemia. Leuk Res [corrected proof, available online 6 January 2009]; in press.

5. Clinical and molecular characterization of a rare syndrome of acute promyelocytic leukemia associated with translocation (11;17);Licht;Blood,1995

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