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An abnormal clone with monosomy 7 and trisomy 21 in the bone marrow of a child with congenital agranulocytosis (Kostmann disease) treated with granulocyte colony-stimulating factor: Evolution towards myelodysplastic syndrome and acute basophilic leukemia
Sofia Shekhter-Levin, Lila Penchansky, Michael R. Wollman, Maureen E. Sherer, Niel Wald, Susanne M. GollinVolume:
84
Year:
1995
Language:
english
Pages:
6
DOI:
10.1016/0165-4608(95)00095-x
File:
PDF, 856 KB
english, 1995