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dc.contributor.author Huret, JL en_US
dc.date.accessioned 2011-11-09T08:54:30Z
dc.date.available 2011-11-09T08:54:30Z
dc.date.issued 2009 en_US
dc.identifier.citation Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2009, Vol. 13, N° 1 ; p. 83 en_US
dc.identifier.issn 1768-3262 en_US
dc.identifier.uri http://hdl.handle.net/2042/44394
dc.description Review on t(9;21)(p22;q22), with data on clinics, and the genes involved. en
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/t0921p22q22ID1304.html en_US
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 en_US
dc.subject Chromosome 9 en_US
dc.subject Chromosome 21 en_US
dc.subject.classification Leukemia Section en_US
dc.subject.classification t-ANLL (class disease) en_US
dc.title t(9;21)(p22;q22) en_US
dc.type Article en_US
dc.contributor.affiliation Jean Loup HURET, Genetics, Dept Medical Information, University of Poitiers en_US
dc.contributor.affiliation CHU Poitiers Hospital, F-86021 Poitiers, France en_US
dc.identifier.doi https://doi.org/10.4267/2042/44394

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