(Q33495063)
Statements
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 (English)
S Shekhter-Levin
L Penchansky
M R Wollman
M E Sherer