Martin Erdel
Linz, Austria
Last Updated: 09/26/2026
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Found 9 publications
Chromosome 1q alterations in transplant-eligible multiple myeloma: clinical impact of copy number and co-occurring high-risk cytogenetic features.
Journal: Frontiers in oncology
Published: May 31, 2026
Functional characterization, localization, and inhibitor sensitivity of the TPR-FGFR1 fusion in 8p11 myeloproliferative syndrome.
Journal: Genes, chromosomes & cancer
Published: March 27, 2015
Switch of the mutation type of the NPM1 gene in acute myeloid leukemia (AML): relapse or secondary AML?
Journal: Blood cancer journal
Published: June 28, 2014
Disruption of the ARID1B and ADAMTS6 loci due to a t(5;6)(q12.3;q25.3) in a patient with developmental delay.
Journal: American journal of medical genetics. Part A
Published: August 17, 2013
Combined Dup(7)(q22.1q32.2), Inv(7)(q31.31q31.33), and Ins(7;19)(q22.1;p13.2p13.2) in a 12-year-old boy with developmental delay and various dysmorphism.
Journal: European journal of medical genetics
Published: November 13, 2012
Single-nucleotide polymorphism array-based characterization of ring chromosome 18.
Journal: The Journal of pediatrics
Published: September 10, 2012
Parental origin of de novo cytogenetically balanced reciprocal non-Robertsonian translocations.
Journal: Cytogenetic and genome research
Published: February 02, 2012
Isolation and characterization of CD133+CD34+VEGFR-2+CD45- fetal endothelial cells from human term placenta.
Journal: Microvascular research
Published: October 28, 2011
Showing 1-9 of 9
Last Updated: 09/26/2026