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Published in 2022 at "Molecular genetics & genomic medicine"
DOI: 10.1002/mgg3.1893
Abstract: To explore the genetic and clinical features of a rare t(1;12)(q21;p13) in a patient with myelodysplastic syndrome (MDS). A 53-year-old male was diagnosed as high-risk MDS, and died in a short period. A complete cytogenetic…
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Keywords:
p13;
q21 p13;
p13 patient;
rare q21 ... See more keywords