t(9;17)(p13;p12) PAX5/NCOR1

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dc.contributor.author Huret, JL en_US
dc.date.accessioned 2015-03-09T10:09:14Z
dc.date.available 2015-03-09T10:09:14Z
dc.date.issued 2015 en_US
dc.identifier.citation Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2015, Vol. 19, N° 3 ; p. 225-226 en_US
dc.identifier.issn 1768-3262
dc.identifier.uri http://hdl.handle.net/2042/56416
dc.description Review on t(9;17)(p13;p12) PAX5/NCOR1, with data on clinics, and the genes involved. en_US
dc.language.iso en en_US
dc.publisher Jean-Loup Huret (Editor-in-Chief) ; INIST-CNRS (Publisher) en_US
dc.relation Atlas of Genetics and Cytogenetics in Oncology and Haematology ; http://AtlasGeneticsOncology.org/Anomalies/t0917p13p12ID1597.html en_US
dc.relation.ispartofseries Atlas of Genetics and Cytogenetics in Oncology and Haematology
dc.rights Open access resource - terms and conditions : http://irevues.inist.fr/utilisation en_US
dc.subject Chromosome 9 en_US
dc.subject Chromosome 17 en_US
dc.subject.classification Leukemia Section en_US
dc.subject.classification B-ALL (class disease) en_US
dc.title t(9;17)(p13;p12) PAX5/NCOR1 en_US
dc.type Article en_US
dc.contributor.affiliation Genetics, Dept Medical Information, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France en_US
dc.identifier.doi https://doi.org/10.4267/2042/56416

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