A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity-Reference-Cited by-同舟云学术

A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity

Published:2012-07 Issue:7-8 Volume:205 Page:365-372
ISSN:2210-7762
Container-title:Cancer Genetics
language:en
Short-container-title:Cancer Genetics

Author:

Jeandidier Eric,Gervais Carine,Radford-Weiss Isabelle,Zink Estelle,Gangneux Catherine,Eischen Alice,Galoisy Anne Cécile,Helias Catherine,Dano Laurent,Cammarata Ornella,Jung Georges,Harzallah Inès,Guérin Eric,Martzolff Lionel,Drénou Bernard,Lioure Bruno,Tancrédi Céline,Rimelen Valérie,Mauvieux Laurent

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

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3. Detection of rare reciprocal RUNX1 rearrangements by next‐generation sequencing in acute myeloid leukemia;Genes, Chromosomes and Cancer;2019-12-02

4. Pediatric acute myeloid leukemia with t(7;21)(p22;q22);Genes, Chromosomes and Cancer;2019-02-14

5. RUNX1-PDCD6 fusion resulting from a novel t(5;21)(p15;q22) chromosome translocation in myelodysplastic syndrome secondary to chronic lymphocytic leukemia;PLOS ONE;2018-04-19