Loci other than 21q22.12 (RUNX1) and 16q21–23.2 cause familial AML
Open Access
- 27 January 2005
- journal article
- research article
- Published by Springer Nature in Leukemia
- Vol. 19 (3) , 465-466
- https://doi.org/10.1038/sj.leu.2403648
Abstract
No abstract availableKeywords
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- Genetic Heterogeneity in Familial Acute Myelogenous Leukemia: Evidence for a Second Locus at Chromosome 16q21-23.2American Journal of Human Genetics, 1997