Recurrence ofOTT-MALfusion in t(1;22) of infant AML-M7-Reference-Cited by-同舟云学术

Recurrence ofOTT-MALfusion in t(1;22) of infant AML-M7

Published:2001-11-08 Issue:1 Volume:33 Page:22-28
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosom. Cancer

Author:

Mercher Thomas,Busson-Le Coniat Maryvonne,Khac Florence Nguyen,Ballerini Paola,Mauchauffé Martine,Bui Hung,Pellegrino Béatrice,Radford Isabelle,Valensi Françoise,Mugneret Francine,Dastugue Nicole,Bernard Olivier A.,Berger Roland

Funder

INSERM

Ligue Nationale Contre le Cancer

Publisher

Wiley

Subject

Cancer Research,Genetics

Reference15 articles.

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2. Nineteen cases of the t(1;22)(p13;q13) acute megakaryoblastic leukaemia of infants/children and a review of 39 cases: report from a t(1;22) study group;Bernstein;Leukemia,2000

3. Distribution of 11q23 breakpoints within the MLL breakpoint cluster region in de novo acute leukemia and in treatment-related acute myeloid leukemia: correlation with scaffold attachment regions and topoisomerase II consensus binding sites;Broeker;Blood,1996

4. The t(1;22) (p13;q13) is nonrandom and restricted to infants with acute megakaryoblastic leukemia: a Pediatric Oncology Group Study;Carroll;Blood,1991

5. Infant acute leukemias show the same biased distribution of ALL1 gene breaks as topoisomerase II related secondary acute leukemias;Cimino;Cancer Res,1997

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