Analysis of common cytogenetic abnormalities in New Zealand pediatric ALL shows ethnically diverse carriage of ETV6-RUNX1, without a corresponding difference in survival
Author:
Affiliation:
1. Children's Haematology Oncology Centre; Christchurch Hospital; Christchurch New Zealand
2. Starship Blood and Cancer Centre; Starship Children's Hospital; Auckland New Zealand
3. National Child Cancer Network NZ; Auckland New Zealand
Funder
New Zealand Children's Cancer Registry
National Child Cancer Network
Publisher
Wiley
Subject
Oncology,Hematology,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/pbc.26676/fullpdf
Reference33 articles.
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2. Pediatric acute lymphoblastic leukemia: where are we going and how do we get there?;Pui;Blood,2012
3. Frequencies of ETV6-RUNX1 fusion and hyperdiploidy in pediatric acute lymphoblastic leukemia are lower in far east than west;Liang;Pediatr Blood Cancer,2010
4. Biologic and clinical characteristics of adolescent and young adult cancers: acute lymphoblastic leukemia, colorectal cancer, breast cancer, melanoma, and sarcoma;Tricoli;Cancer,2016
5. Cytogenetics of paediatric and adolescent acute lymphoblastic leukaemia;Harrison;Br J Haematol,2009
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1. The Prenatal Origin of Childhood Leukemia: Potential Applications for Epidemiology and Newborn Screening;Frontiers in Pediatrics;2021-04-23
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3. Insights into the prenatal origin of childhood acute lymphoblastic leukemia;Cancer and Metastasis Reviews;2020-01-04
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