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

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URI: http://hdl.handle.net/2042/70534  |   DOI : https://doi.org/10.4267/2042/70534
Title: t(20;21)(q11;q22) RUNX1/NOL4L
Author: Huret, Jean Loup
Abstract: Review on t(20;21)(q11;q22), with data on clinics, and the genes involved.
Subject: Chromosome 20; Chromosome 21; Acute myeloid leukemia; Chronic myelogenous leukaemia; RUNX1/NOL4L; Leukaemia Section; Adolescent; Adult; Aged; Aged, 80 and over; Child; Child, Preschool; *Chromosome Aberrations; Chromosomes, Human, Pair 21/*genetics; Cooperative Behavior; Core Binding Factor Alpha 2 Subunit/*genetics; Female; France/epidemiology; Hematologic Diseases/epidemiology/*genetics/pathology; Humans; Karyotyping; Male; Middle Aged; Retrospective Studies; *Translocation, Genetic; Adult; *Chromosomes, Human, Pair 20
Publisher: ARMGHM - Atlas Génétique des Cancers
Date: 2019

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