A pediatric case of acute myeloid leukemia with KMT2A gene rearrangement t(10;11) and 16p11.2 microdeletion syndrome
Year: 2020
Type: article
Source: Pediatric Blood & Cancer
DOI: 10.1002/pbc.28764
Institution: University of Hawaiʻi at Mānoa
Language: English
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W3093185193
