Title of article :
Translocation (2;3)(p21;q26) as the Sole Anomaly in a Case of Primary Myelofibrosis
Author/Authors :
Christian Herens، نويسنده , , Christian and Hermanne، نويسنده , , Jean-Philippe and Tassin، نويسنده , , Francoise and Fassotte، نويسنده , , Marie France and Thiry، نويسنده , , Albert and Jamar، نويسنده , , Mauricette and Schaaf-Lafontaine، نويسنده , , Nicole and Fillet، نويسنده , , Georges and Koulischer، نويسنده , , Lucien، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 1999
Pages :
3
From page :
62
To page :
64
Abstract :
Translocation t(2p;3q) is a rare but recurrent finding in myeloid disorders. We present the first case of primary myelofibrosis with t(2;3)(p21;q26) as the sole chromosomal anomaly. The comparison with the 11 other previously published myeloid-associated t(2p;3q) cases confirms that this nonrandom translocation involves a pluripotent stem cell and is associated with a poor prognosis.
Journal title :
Cancer Genetics and Cytogenetics
Serial Year :
1999
Journal title :
Cancer Genetics and Cytogenetics
Record number :
1821896
Link To Document :
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