t(2;3)(p15-23;q26-27)

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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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