t(9;11)(q34;q23) FBP17/MLL

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dc.contributor.author Fuchs, U fr_FR
dc.contributor.author Borkhardt, A fr_FR
dc.date.accessioned 2011-02-22T15:10:30Z
dc.date.available 2011-02-22T15:10:30Z
dc.date.issued 2001 fr_FR
dc.identifier.citation Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2001, Vol. 5, N° 3 ; p. 201-202 fr_FR
dc.identifier.issn 1768-3262
dc.identifier.uri http://hdl.handle.net/2042/37761
dc.description Review on t(9;11)(q34;q23) FBP17/MLL, 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/t0911FBPID1205.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 9 fr_FR
dc.subject Chromosome 11 fr_FR
dc.subject ins(11;9)(q23;q34)inv(11)(q13;q23) (alias) fr_FR
dc.subject.classification Leukemia Section fr_FR
dc.subject.classification ANLL (class disease) fr_FR
dc.subject.mesh FNBP1 protein, human fr_FR
dc.subject.mesh Chromosome Aberrations fr_FR
dc.subject.mesh Leukemia, Myeloid, Acute fr_FR
dc.subject.mesh Translocation, Genetic fr_FR
dc.title t(9;11)(q34;q23) FBP17/MLL fr_FR
dc.type Short Communication fr_FR
dc.contributor.affiliation Children's University Hospital Giessen, Hematology &Oncology, Feulgenstr. 12, 35392 Giessen, Germany fr_FR
dc.identifier.doi https://doi.org/10.4267/2042/37761


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