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dc.contributor.author Bojesen, SE fr_FR
dc.date.accessioned 2011-02-22T15:13:06Z
dc.date.available 2011-02-22T15:13:06Z
dc.date.issued 2001 fr_FR
dc.identifier.citation Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2001, Vol. 5, N° 4 ; p. 291-292 fr_FR
dc.identifier.issn 1768-3262 fr_FR
dc.identifier.uri http://hdl.handle.net/2042/37793
dc.description Review on t(X;11)(q13;q23), 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/t0X11ID1127.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 X fr_FR
dc.subject Chromosome 11 fr_FR
dc.subject.classification Leukemia Section fr_FR
dc.subject.classification ANLL (class disease) fr_FR
dc.subject.classification T-ALL (class disease) fr_FR
dc.subject.mesh FOXO4 protein, human fr_FR
dc.subject.mesh Chromosome Aberrations fr_FR
dc.subject.mesh Leukemia fr_FR
dc.subject.mesh Leukemia, Lymphoid fr_FR
dc.subject.mesh Lymphoproliferative Disorders fr_FR
dc.subject.mesh Precursor Cell Lymphoblastic Leukemia-Lymphoma fr_FR
dc.subject.mesh Translocation, Genetic fr_FR
dc.title t(X;11)(q13;q23) fr_FR
dc.type Short Communication fr_FR
dc.contributor.affiliation Department of Clinical Biochemistry, Herlev University Hospital, Herlev Ringvej 75, Herlev DK-2730, Denmark fr_FR
dc.identifier.doi https://doi.org/10.4267/2042/37793

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