L Michaux1, J Dierlamm, C Mecucci
1Center for Human Genetics, Katholieke Universiteit Leuven, Belgium.
Researchers identified a specific chromosomal anomaly, dic(1;15)(p11;p11), in three myeloid disorder cases. This finding suggests a reclassification of six previously reported t(1;15) cases, highlighting a common genetic abnormality in myeloid disorders.
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