t(1;14)(q21;q32) FCGR2B/IGH

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dc.contributor.author Boyer, J fr_FR
dc.date.accessioned 2011-02-22T15:46:38Z
dc.date.available 2011-02-22T15:46:38Z
dc.date.issued 2005 fr_FR
dc.identifier.citation Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2005, Vol. 9, N° 2 ; p. 155 fr_FR
dc.identifier.issn 1768-3262 fr_FR
dc.identifier.uri http://hdl.handle.net/2042/38191
dc.description Review on t(1;14)(q21;q32) FCGR2B/IGH, 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/t0114q21q32ID1341.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 14 fr_FR
dc.subject.classification Leukemia Section fr_FR
dc.subject.classification NHL (class disease) fr_FR
dc.subject.mesh FCGR2B protein, human fr_FR
dc.subject.mesh Chromosome Aberrations fr_FR
dc.subject.mesh Lymphoma, Follicular fr_FR
dc.subject.mesh Lymphoma, Non-Hodgkin fr_FR
dc.subject.mesh Lymphoproliferative Disorders fr_FR
dc.subject.mesh Translocation, Genetic fr_FR
dc.title t(1;14)(q21;q32) FCGR2B/IGH 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/10.4267/2042/38191

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