TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis (Q71020950)
scientific article published on 01 December 1995
| Language | Label | Description | Also known as |
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| English | TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis |
scientific article published on 01 December 1995 |
Statements
TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis (English)
Shurtleff SA
Buijs A
Behm FG
Rubnitz JE
Raimondi SC
Hancock ML
Pui CH
Grosveld G
1 December 1995