A newborn with congenital mixed phenotype acute leukemia with complex translocation t(10;11)(p12;q23) with KMT2A/MLLT10 rearranged – a report of an extremely rare case-Reference-Cited by-同舟云学术

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A newborn with congenital mixed phenotype acute leukemia with complex translocation t(10;11)(p12;q23) with KMT2A/MLLT10 rearranged – a report of an extremely rare case

Published:2018 Issue:3 Volume:43 Page:346-352
ISSN:1426-3912
Container-title:Central European Journal of Immunology
language:
Short-container-title:cejoi

Author:

Szpecht Dawid,Skalska-Sadowska Jolanta,Michniewicz Barbara,Gadzinowski Janusz,Machowska Ludmiła,Pieczonka Anna,Przybyłowicz-Chalecka Anna,Kanduła Zuzanna,Jarmuż-Szymczak Małgorzata,Lewandowski Krzysztof,Wachowiak Jacek

Publisher

Termedia Sp. z.o.o.

Subject

Immunology,Immunology and Allergy

Cited by 1 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. An alternative approach to confirm mixed lineage involvement in acute leukemia with KMT2A rearrangement–an illustrative report;Blood Research;2023-06-30

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