t(7;12)(q36;p13)

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dc.contributor.author Huret, JL fr_FR
dc.date.accessioned 2011-02-22T14:58:32Z
dc.date.available 2011-02-22T14:58:32Z
dc.date.issued 2000 fr_FR
dc.identifier.citation Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2000, Vol. 4, N° 2 ; p. 80 fr_FR
dc.identifier.issn 1768-3262 fr_FR
dc.identifier.uri http://hdl.handle.net/2042/37620
dc.description Review on t(7;12)(q36;p13), 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/t0712ID1177.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 7 fr_FR
dc.subject Chromosome 12 fr_FR
dc.subject.classification Leukemia Section fr_FR
dc.subject.classification MDS (class disease) fr_FR
dc.subject.classification ANLL (class disease) fr_FR
dc.subject.classification B-ALL (class disease) fr_FR
dc.subject.mesh ETS translocation variant 6 protein fr_FR
dc.subject.mesh Chromosome Aberrations fr_FR
dc.subject.mesh Translocation, Genetic fr_FR
dc.title t(7;12)(q36;p13) 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/10.4267/2042/37620


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