| dc.contributor.author |
Stevens-Kroef, M |
fr_FR |
| dc.date.accessioned |
2011-02-22T15:39:40Z |
|
| dc.date.available |
2011-02-22T15:39:40Z |
|
| dc.date.issued |
2004 |
fr_FR |
| dc.identifier.citation |
Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2004, Vol. 8, N° 3 ; p. 251-252 |
fr_FR |
| dc.identifier.issn |
1768-3262 |
|
| dc.identifier.uri |
http://hdl.handle.net/2042/38111 |
|
| dc.description |
Review on t(2;3)(p15-23;q26-27), with data on clinics, and the genes involved. |
en |
| dc.language.iso |
en |
fr_FR |
| dc.publisher |
Jean-Loup Huret (Editor-in-Chief) ; INIST-CNRS (Publisher) |
fr_FR |
| dc.relation |
Atlas of Genetics and Cytogenetics in Oncology and Haematology ; http://AtlasGeneticsOncology.org//Anomalies/t0203p23q26ID1274.html |
fr_FR |
| dc.relation.ispartofseries |
Atlas of Genetics and Cytogenetics in Oncology and Haematology |
|
| dc.rights |
Open access resource - terms and conditions : http://documents.irevues.inist.fr/utilisation |
fr_FR |
| dc.subject |
Chromosome 2 |
fr_FR |
| dc.subject |
Chromosome 3 |
fr_FR |
| dc.subject.classification |
Leukemia Section |
fr_FR |
| dc.subject.classification |
MPD (class disease) |
fr_FR |
| dc.subject.classification |
MDS (class disease) |
fr_FR |
| dc.subject.classification |
t-ANLL (class disease) |
fr_FR |
| dc.subject.mesh |
EVI1 protein, human |
fr_FR |
| dc.subject.mesh |
Anemia, Refractory |
fr_FR |
| dc.subject.mesh |
Anemia, Refractory, with Excess of Blasts |
fr_FR |
| dc.subject.mesh |
Anemia, Sideroblastic |
fr_FR |
| dc.subject.mesh |
Bone Marrow Diseases |
fr_FR |
| dc.subject.mesh |
Chromosome Aberrations |
fr_FR |
| dc.subject.mesh |
Leukemia, Myeloid |
fr_FR |
| dc.subject.mesh |
Leukemia, Myeloid, Acute |
fr_FR |
| dc.subject.mesh |
Leukemia, Myelomonocytic, Chronic |
fr_FR |
| dc.subject.mesh |
Myelodysplastic Syndromes |
fr_FR |
| dc.subject.mesh |
Myelodysplastic-Myeloproliferative Diseases |
fr_FR |
| dc.subject.mesh |
Translocation, Genetic |
fr_FR |
| dc.title |
t(2;3)(p15-23;q26-27) |
fr_FR |
| dc.type |
Mini Review |
fr_FR |
| dc.contributor.affiliation |
Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands |
fr_FR |
| dc.identifier.doi |
https://doi.org/10.4267/2042/38111 |
|
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