Matches in Nanopublications for { ?s ?p "[In this series of unselected patients, LOH of ETV6 markers was found in 23% of cases (6% of T-ALL and 26% of B lineage ALL) confirming that chromosome 12p12-13 deletions represent a major genetic alteration in childhood ALL, frequently missed by cytogenetic analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 1 of
1
with 100 items per page.
- NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_assertion description "[In this series of unselected patients, LOH of ETV6 markers was found in 23% of cases (6% of T-ALL and 26% of B lineage ALL) confirming that chromosome 12p12-13 deletions represent a major genetic alteration in childhood ALL, frequently missed by cytogenetic analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164015.RAHSLo_JzyMs-48Q2ibR7lTLhZHcdJ0w4VRRPDZ-Ss-Xg130_provenance.