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dc.contributor.author Pébusque, MJ fr_FR
dc.date.accessioned 2011-02-22T15:05:25Z
dc.date.available 2011-02-22T15:05:25Z
dc.date.issued 2001 fr_FR
dc.identifier.citation Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2001, Vol. 5, N° 1 ; p. 37-38 fr_FR
dc.identifier.issn 1768-3262
dc.identifier.uri http://hdl.handle.net/2042/37703
dc.description Review on t(6;8)(q27;p12), 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/t68ID1090.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 6 fr_FR
dc.subject Chromosome 8 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 NHL (class disease) fr_FR
dc.subject.mesh FGFR1 protein, human fr_FR
dc.subject.mesh Bone Marrow Diseases fr_FR
dc.subject.mesh Chromosome Aberrations fr_FR
dc.subject.mesh Lymphoma, Non-Hodgkin fr_FR
dc.subject.mesh Lymphoproliferative Disorders fr_FR
dc.subject.mesh Myeloproliferative Disorders fr_FR
dc.subject.mesh Primary Myelofibrosis fr_FR
dc.subject.mesh Translocation, Genetic fr_FR
dc.title t(6;8)(q27;p12) fr_FR
dc.type Mini Review fr_FR
dc.contributor.affiliation INSERM U119, IFR 57, 27 Blvd Leï Roure, 13009 Marseille, France fr_FR
dc.identifier.doi https://doi.org/10.4267/2042/37703

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