Claudia J. Erpelinck
Rotterdam, ZH, Netherlands
Last Updated: 09/26/2026
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Found 11 publications
MDS/AML and AML with myelodysplasia-related gene mutations: clinical and molecular similarities.
Journal: Blood advances
Published: September 11, 2025
MDS/AML and AML with myelodysplasia-related gene mutations: clinical and molecular similarities.
Journal: Blood advances
Published: September 11, 2025
Allele-specific expression of GATA2 due to epigenetic dysregulation in CEBPA double-mutant AML.
Journal: Blood
Published: September 28, 2020
Atypical 3q26/MECOM rearrangements genocopy inv(3)/t(3;3) in acute myeloid leukemia.
Journal: Blood
Published: October 11, 2019
Lethal neonatal bone marrow failure syndrome with multiple congenital abnormalities, including limb defects, due to a constitutional deletion of 3' MECOM.
Journal: Haematologica
Published: February 14, 2018
An autonomous CEBPA enhancer specific for myeloid-lineage priming and neutrophilic differentiation.
Journal: Blood
Published: January 28, 2016
Congenital thrombocytopenia in a neonate with an interstitial microdeletion of 3q26.2q26.31.
Journal: American journal of medical genetics. Part A
Published: March 23, 2015
Deregulated expression of EVI1 defines a poor prognostic subset of MLL-rearranged acute myeloid leukemias: a study of the German-Austrian Acute Myeloid Leukemia Study Group and the Dutch-Belgian-Swiss HOVON/SAKK Cooperative Group.
Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Published: September 26, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026