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

Autor: Shekhter-Levin, S., Penchansky, L., Wallman, M. R., Sherer, M. E., Wald, N., Gollin, S. M.
Zdroj: Cancer Genetics and Cytogenetics; 1995, Vol. 84 Issue: 2 p99-104, 6p
Databáze: Supplemental Index