t(1;22)(p13;q13)

Show simple item record

dc.contributor.author Huret, JL en_US
dc.date.accessioned 2010-05-12T09:11:50Z
dc.date.available 2010-05-12T09:11:50Z
dc.date.issued 1997 en_US
dc.identifier.citation Atlas of Genetics and Cytogenetics in Oncology and Haematology; 1997, Vol. 1, N° 1 ; p. 17 en_US
dc.identifier.uri http://hdl.handle.net/2042/32029
dc.description Review on t(1;22)(p13;q13), 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/t0122.html en_US
dc.relation.ispartofseries Atlas of Genetics and Cytogenetics in Oncology and Haematology
dc.subject Chromosome 1 en_US
dc.subject Chromosome 22 en_US
dc.subject.classification ANLL (class disease) en_US
dc.subject.classification Leukemia Section en_US
dc.subject.mesh Chromosome Disorders en_US
dc.subject.mesh MKL1 protein, human en_US
dc.subject.mesh Chromosome Aberrations en_US
dc.subject.mesh Abnormalities, Multiple en_US
dc.subject.mesh Translocation, Genetic en_US
dc.subject.mesh Mental Retardation en_US
dc.subject.mesh Leukemia, Myeloid, Acute en_US
dc.subject.mesh Down Syndrome en_US
dc.title t(1;22)(p13;q13) en_US
dc.type Article en_US
dc.contributor.affiliation Genetics, Dept Medical Information, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France en_US
dc.identifier.doi https://doi.org/10.4267/2042/32029


Files in this item

PDF 08-1997-t0122.pdf 15.18Kb

This item appears in the following Collection(s)

Show simple item record





Advanced Search