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dc.contributor.author Van, den Akker J en_US
dc.contributor.author Huret, JL en_US
dc.date.accessioned 2010-05-12T09:48:33Z
dc.date.available 2010-05-12T09:48:33Z
dc.date.issued 1997 en_US
dc.identifier.citation Atlas of Genetics and Cytogenetics in Oncology and Haematology; 1997, Vol. 1, N° 2 ; p. 81-82 en_US
dc.identifier.issn 1768-3262
dc.identifier.uri http://hdl.handle.net/2042/32063
dc.description Review on t(12;22)(p13;q11-12), with data on clinics, and the genes involved. en
dc.language.iso en en_US
dc.publisher Jean-Loup Huret (Editor-in-Chief) ; INIST-CNRS (Publisher) en_US
dc.relation Atlas of Genetics and Cytogenetics in Oncology and Haematology ; http://AtlasGeneticsOncology.org//Anomalies/t1222.html en_US
dc.relation.ispartofseries Atlas of Genetics and Cytogenetics in Oncology and Haematology
dc.subject Chromosome 22 en_US
dc.subject Chromosome 12 en_US
dc.subject.classification ANLL (class disease) en_US
dc.subject.classification Leukemia Section en_US
dc.subject.classification MDS (class disease) en_US
dc.subject.classification MPD (class disease) en_US
dc.subject.mesh Translocation, Genetic en_US
dc.subject.mesh Myelodysplastic Syndromes en_US
dc.subject.mesh Leukemia en_US
dc.subject.mesh Chromosome Aberrations en_US
dc.subject.mesh Bone Marrow Diseases en_US
dc.subject.mesh ETS translocation variant 6 protein en_US
dc.title t(12;22)(p13;q11-12) en_US
dc.type Article en_US
dc.contributor.affiliation Genetics, Dept Medical Information, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France (JLH) en_US
dc.contributor.affiliation Laboratoire De Cytogenetique, Hôpital Saint-Antoine, 184 rue du Faubourg Saint-Antoine, 75571 Paris, Cedex 12, France (JVDA) en_US
dc.identifier.doi https://doi.org/10.4267/2042/32063

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