inv(16)(p13q22) - t(16;16)(p13;q22) - del(16)(q22)

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dc.contributor.author Huret, JL fr_FR
dc.date.accessioned 2011-02-22T14:51:52Z
dc.date.available 2011-02-22T14:51:52Z
dc.date.issued 1999 fr_FR
dc.identifier.citation Atlas of Genetics and Cytogenetics in Oncology and Haematology; 1999, Vol. 3, N° 3 ; p. 147-149 fr_FR
dc.identifier.issn 1768-3262 fr_FR
dc.identifier.uri http://hdl.handle.net/2042/37539
dc.description Review on inv(16)(p13q22) - t(16;16)(p13;q22) - del(16)(q22), 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/inv16.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 16 fr_FR
dc.subject.classification Leukemia Section fr_FR
dc.subject.classification MPD (class disease) fr_FR
dc.subject.classification MDS (class disease) fr_FR
dc.subject.classification ANLL (class disease) fr_FR
dc.subject.classification t-ANLL (class disease) fr_FR
dc.subject.mesh CBFB protein, human fr_FR
dc.subject.mesh Chromosome Aberrations fr_FR
dc.subject.mesh Chromosome Deletion fr_FR
dc.subject.mesh Inversion, Chromosome fr_FR
dc.subject.mesh Loss of Heterozygosity fr_FR
dc.subject.mesh Translocation, Genetic fr_FR
dc.title inv(16)(p13q22) - t(16;16)(p13;q22) - del(16)(q22) fr_FR
dc.type Mini Review fr_FR
dc.contributor.affiliation Genetics, Dept Medical Information, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France fr_FR
dc.identifier.doi https://doi.org/10.4267/2042/37539


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