A novel cryptic CBFB-MYH11 gene fusion present at birth leading to acute myeloid leukemia and allowing molecular monitoring for minimal residual disease-Reference-Cited by-同舟云学术

A novel cryptic CBFB-MYH11 gene fusion present at birth leading to acute myeloid leukemia and allowing molecular monitoring for minimal residual disease

Published:2018-03 Issue: Volume:11 Page:34-38
ISSN:2214-3300
Container-title:Human Pathology: Case Reports
language:en
Short-container-title:Human Pathology: Case Reports

Author:

Poddighe P.J.,Veening M.A.,Mansur M.B.,Loonen A.H.,Westers T.M.,Merle P.A.,Wessels J.W.,de Haas V.,Kors W.A.,Bhola S.L.,Wondergem M.J.,Ford A.M.,Kaspers G.J.L.

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference15 articles.

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3. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia;Arber;Blood,2016

4. Results of a randomized trial in children with acute myeloid leukaemia: medical research council AML12 trial;Gibson;Br. J. Haematol.,2011

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Rare type I CBFβ/MYH11 fusion transcript in primary acute myeloid leukemia with inv(16)(p13.1q22): a case report;Brazilian Journal of Medical and Biological Research;2021

2. Advancements in Next-Generation Sequencing for Detecting Minimal Residual Disease;Minimal Residual Disease Testing;2018-11-16

3. Preleukemia and Leukemia-Initiating Cell Activity in inv(16) Acute Myeloid Leukemia;Frontiers in Oncology;2018-04-26