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

✍ Scribed by Sofia Shekhter-Levin; Lila Penchansky; Michael R. Wollman; Maureen E. Sherer; Niel Wald; Susanne M. Gollin

• Book ID: 113253577
• Publisher: Elsevier Science
• Year: 1995
• Tongue: English
• Weight: 856 KB
• Volume: 84
• Category: Article
• ISSN: 0165-4608
• DOI: 10.1016/0165-4608(95)00095-x