t(2;3)(p23;q21)

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dc.contributor.author Huret, JL fr_FR
dc.date.accessioned 2011-02-22T15:12:45Z
dc.date.available 2011-02-22T15:12:45Z
dc.date.issued 2001 fr_FR
dc.identifier.citation Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2001, Vol. 5, N° 4 ; p. 287-288 fr_FR
dc.identifier.issn 1768-3262
dc.identifier.uri http://hdl.handle.net/2042/37789
dc.description Review on t(2;3)(p23;q21), 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/t0203ID1217.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 NHL (class disease) fr_FR
dc.subject.mesh TFG protein, human fr_FR
dc.subject.mesh Chromosome Aberrations fr_FR
dc.subject.mesh Lymphoma, B-Cell fr_FR
dc.subject.mesh Lymphoma, Large B-Cell, Diffuse fr_FR
dc.subject.mesh Lymphoma, Non-Hodgkin fr_FR
dc.subject.mesh Lymphoproliferative Disorders fr_FR
dc.subject.mesh Translocation, Genetic fr_FR
dc.title t(2;3)(p23;q21) fr_FR
dc.type Mini Review fr_FR
dc.contributor.affiliation Genetics, Dept Medical Information, UMR 8125 CNRS, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France       fr_FR
dc.identifier.doi https://doi.org/10.4267/2042/37789


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