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| Reference : Translocation (2;3)(p21;q26) as the sole anomaly in a case of primary myelofibrosis. |
| Scientific journals : Article | |||
| Life sciences : Genetics & genetic processes | |||
| http://hdl.handle.net/2268/16518 | |||
| Translocation (2;3)(p21;q26) as the sole anomaly in a case of primary myelofibrosis. | |
| English | |
Herens, Christian  [Centre Hospitalier Universitaire de Liège - CHU > > Génétique >] | |
| Hermanne, Jean-Philippe [Centre Hospitalier Universitaire de Liège - CHU >] | |
| Tassin, Françoise [Centre Hospitalier Universitaire de Liège - CHU > > Hématologie biologique et immuno hématologie >] | |
| Fassotte, Marie-France [Centre Hospitalier Universitaire de Liège - CHU > > Hématologie clinique >] | |
| Thiry, Albert [Université de Liège - ULg > > Anatomie pathologique >] | |
| Jamar, Mauricette [Université de Liège - ULg > > Génétique >] | |
| Schaaf, Nicole [Centre Hospitalier Universitaire de Liège - CHU > > Hématologie biologique et immuno hématologie >] | |
| Fillet, Georges [Centre Hospitalier Universitaire de Liège - CHU > > Hématologie clinique >] | |
| Koulischer, Lucien [> > > >] | |
| 1999 | |
| Cancer Genetics & Cytogenetics | |
| Elsevier Science | |
| 110 | |
| 1 | |
| 62-4 | |
| 0165-4608 | |
| 1873-4456 | |
| New York | |
| NY | |
| [en] Aged ; Chromosomes, Human, Pair 2 ; Chromosomes, Human, Pair 3 ; Humans ; Male ; Primary Myelofibrosis/genetics ; Translocation, Genetic | |
| [en] 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. | |
| http://hdl.handle.net/2268/16518 |
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