A pediatric case of acute myeloid leukemia with KMT2A gene rearrangement t(10;11) and 16p11.2 microdeletion syndrome-Reference-Cited by-同舟云学术

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A pediatric case of acute myeloid leukemia with KMT2A gene rearrangement t(10;11) and 16p11.2 microdeletion syndrome

Published:2020-10-15 Issue:2 Volume:68 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Abe Keisuke¹^ORCID,Dowsett Leah¹,Wada Randal¹,Hutchins Kelley¹

Affiliation:

1. Department of Pediatrics University of Hawai'i John A. Burns School of Medicine Honolulu Hawaii

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.28764

Reference23 articles.

1. Current Management of Childhood Acute Myeloid Leukemia

2. Pediatric acute myeloid leukemia: updates on biology, risk stratification, and therapy

3. Diagnosis and management of acute myeloid leukemia in children and adolescents: recommendations from an international expert panel

4. Bloom's Syndrome: Clinical Spectrum, Molecular Pathogenesis, and Cancer Predisposition

5. Down syndrome and AML: where do we go from here?

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. Further Delineation of the Proximal 16p11.2 Microdeletion Syndrome: Novel Findings Among 22 New Individuals;American Journal of Medical Genetics Part A;2024-09-11

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