t(20;21)(q11;q22) RUNX1/NOL4L

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dc.contributor.author Huret, Jean Loup -
dc.date.accessioned 2019-11-05T12:12:20Z
dc.date.available 2019-11-05T12:12:20Z
dc.date.issued 2019 -
dc.identifier.citation Jean Loup, Huret. t(20;21)(q11;q22) RUNX1/NOL4L. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2019, 9, p. 295-296 -
dc.identifier.issn 1768-3262
dc.identifier.uri http://hdl.handle.net/2042/70534
dc.description.abstract Review on t(20;21)(q11;q22), with data on clinics, and the genes involved. en
dc.language.iso en -
dc.publisher ARMGHM - Atlas Génétique des Cancers -
dc.relation Atlas of Genetics and Cytogenetics in Oncology and Haematology ; http://AtlasGeneticsOncology.org/Anomalies/t2021q11q22ID1307.html -
dc.relation.ispartofseries Atlas of Genetics and Cytogenetics in Oncology and Haematology en
dc.rights Open access resource - terms and conditions : http://irevues.inist.fr/utilisation -
dc.subject Chromosome 20 en
dc.subject Chromosome 21 en
dc.subject Acute myeloid leukemia en
dc.subject Chronic myelogenous leukaemia en
dc.subject RUNX1/NOL4L en
dc.subject.classification Leukaemia Section en
dc.subject.mesh Adolescent en
dc.subject.mesh Adult en
dc.subject.mesh Aged en
dc.subject.mesh Aged, 80 and over en
dc.subject.mesh Child en
dc.subject.mesh Child, Preschool en
dc.subject.mesh *Chromosome Aberrations en
dc.subject.mesh Chromosomes, Human, Pair 21/*genetics en
dc.subject.mesh Cooperative Behavior en
dc.subject.mesh Core Binding Factor Alpha 2 Subunit/*genetics en
dc.subject.mesh Female en
dc.subject.mesh France/epidemiology en
dc.subject.mesh Hematologic Diseases/epidemiology/*genetics/pathology en
dc.subject.mesh Humans en
dc.subject.mesh Karyotyping en
dc.subject.mesh Male en
dc.subject.mesh Middle Aged en
dc.subject.mesh Retrospective Studies en
dc.subject.mesh *Translocation, Genetic en
dc.subject.mesh Adult en
dc.subject.mesh *Chromosomes, Human, Pair 20 en
dc.title t(20;21)(q11;q22) RUNX1/NOL4L en
dc.type Article -
dc.identifier.doi https://doi.org/10.4267/2042/70534

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