t(8;19)(p11;q13)

Show simple item record

dc.contributor.author Boyer, J fr_FR
dc.date.accessioned 2011-02-22T15:36:38Z
dc.date.available 2011-02-22T15:36:38Z
dc.date.issued 2004 fr_FR
dc.identifier.citation Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2004, Vol. 8, N° 2 ; p. 91-92 fr_FR
dc.identifier.issn 1768-3262
dc.identifier.uri http://hdl.handle.net/2042/38074
dc.description Review on t(8;19)(p11;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/t0819p11q13ID1315.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 8 fr_FR
dc.subject Chromosome 19 fr_FR
dc.subject.classification Leukemia Section fr_FR
dc.subject.classification ANLL (class disease) fr_FR
dc.subject.mesh MYST3 protein, human fr_FR
dc.subject.mesh Chromosome Aberrations fr_FR
dc.subject.mesh Leukemia, Monocytic, Acute fr_FR
dc.subject.mesh Leukemia, Myeloid fr_FR
dc.subject.mesh Leukemia, Myeloid, Acute fr_FR
dc.subject.mesh Leukemia, Myelomonocytic, Acute fr_FR
dc.subject.mesh Translocation, Genetic fr_FR
dc.title t(8;19)(p11;q13) fr_FR
dc.type Short Communication fr_FR
dc.contributor.affiliation Laboratoire d'Hématologie, CH du MANS, France fr_FR
dc.identifier.doi https://doi.org/10.4267/2042/38074


Files in this item

PDF 12-2003-t0819p11q13ID1315.pdf 18.88Kb

This item appears in the following Collection(s)

Show simple item record





Advanced Search