t(3;11)(q26;p15)

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dc.contributor.author Huret, JL fr_FR
dc.date.accessioned 2011-02-22T16:11:42Z
dc.date.available 2011-02-22T16:11:42Z
dc.date.issued 2008 fr_FR
dc.identifier.citation Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2008, Vol. 12, N° 1 ; p. 60 fr_FR
dc.identifier.issn 1768-3262 fr_FR
dc.identifier.uri http://hdl.handle.net/2042/38480
dc.description Review on t(3;11)(q26;p15), 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/t0311q26p15ID1474.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 3 fr_FR
dc.subject Chromosome 11 fr_FR
dc.subject.classification Leukemia Section fr_FR
dc.subject.classification MPD (class disease) fr_FR
dc.subject.mesh EVI1 protein, human 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, Myelomonocytic, Chronic fr_FR
dc.subject.mesh Myelodysplastic-Myeloproliferative Diseases fr_FR
dc.subject.mesh Translocation, Genetic fr_FR
dc.title t(3;11)(q26;p15) fr_FR
dc.type Short Communication fr_FR
dc.contributor.affiliation Genetics, Dept Medical Information, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France fr_FR
dc.identifier.doi https://doi.org/10.4267/2042/38480


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