U. Jacobs

Analysis of t(9;11) chromosomal breakpoint sequences in childhood acute leukemia: Almost identical MLL breakpoints in therapy‐related AML after treatment without etoposides

A. Borkhardt, J. Harbott, M. Schrappe, 2003, Genes, chromosomes & cancer.

Bladder exstrophy and Epstein type congenital macrothrombocytopenia: Evidence for a common cause?

J. Martignetti, A. Difeo, J. Dötsch, 2006, American journal of medical genetics. Part A.

Bimodal distribution of genomic MLL breakpoints in infant acute lymphoblastic leukemia treatment

M. D. Boer, R. Pieters, A. Teigler‐Schlegel, 2010, Leukemia.

Cluster analysis of genomic ETV6-RUNX1 (TEL-AML1) fusion sites in childhood acute lymphoblastic leukemia.

J. V. van Dongen, V. V. D. van der Velden, J. Harbott, 2009, Leukemia research.

Infantile hypophosphatasia due to a new compound heterozygous TNSALP mutation - functional evidence for a hydrophobic side-chain?

J. Dötsch, H. Dörr, W. Rascher, 2008, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Identification of the genomic BCR-ABL1 fusion sequence from blood specimen stored on filter paper.

M. Metzler, M. Suttorp, M. Krumbholz, 2013, Leukemia research.