Genetic Heterogeneity in Familial Acute Myelogenous Leukemia: Evidence for a Second Locus at Chromosome 16q21-23.2

Marshall S. Horwitz(University of Washington), Wendy H. Raskind(Pacific Northwest Diabetes Research Institute), Marie Mangelsdorf(Women's and Children's Hospital), Kathleen F. Benson(University of Washington), Lynne Hobson(South Australia Pathology), John Wolff(University of Washington), D. Hewett(Boston Children's Hospital), Sui Yu(Boston Children's Hospital), Robert I. Richards(University of South Australia), Feng-Qian Li(University of Washington), Mark Leppert(Howard Hughes Medical Institute)
The American Journal of Human Genetics
October 1, 1997
10.1086/514894
Cited by 43

Related Papers

Isolation of a Common Receptor for Coxsackie B Viruses and Adenoviruses 2 and 5
|Science|1997|3.1k
Neutrophil Elastase, Proteinase 3, and Cathepsin G as Therapeutic Targets in Human Diseases
|Pharmacological Reviews|2010|857
Whole-organism lineage tracing by combinatorial and cumulative genome editing
|Science|2016|826
Localization of an ataxia-telangiectasia gene to chromosome 11q22–23
|Nature|1988|687
Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia
|Nature Genetics|2011|604