t(1;22)(p13;q13)

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dc.contributor.author Huret, JL fr_FR
dc.date.accessioned 2011-02-22T15:10:20Z
dc.date.available 2011-02-22T15:10:20Z
dc.date.issued 2001 fr_FR
dc.identifier.citation Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2001, Vol. 5, N° 3 ; p. 193-194 fr_FR
dc.identifier.issn 1768-3262
dc.identifier.uri http://hdl.handle.net/2042/37759
dc.description Review on t(1;22)(p13;q13), 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/t0122.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 1 fr_FR
dc.subject Chromosome 22 fr_FR
dc.subject.classification Leukemia Section fr_FR
dc.subject.classification ANLL (class disease) fr_FR
dc.subject.mesh MKL1 protein, human fr_FR
dc.subject.mesh Abnormalities, Multiple fr_FR
dc.subject.mesh Chromosome Aberrations fr_FR
dc.subject.mesh Chromosome Disorders fr_FR
dc.subject.mesh Down Syndrome fr_FR
dc.subject.mesh Leukemia, Myeloid, Acute fr_FR
dc.subject.mesh Mental Retardation fr_FR
dc.subject.mesh Translocation, Genetic fr_FR
dc.title t(1;22)(p13;q13) fr_FR
dc.type Mini Review fr_FR
dc.contributor.affiliation Genetics, Dept Medical Information, UMR 8125 CNRS, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France       fr_FR
dc.identifier.doi https://doi.org/10.4267/2042/37759


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