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
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Current Data About 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
(P31) (Q13442814)
(P248)
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(P813) Tuesday, October 15, 2019

(P50) (Q71020949)
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(P304) 1985-1989
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(P478) 9
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(P577) Friday, December 1, 1995
(P248)
(P698) 8609706
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(P813) Tuesday, October 15, 2019

(P1433) (Q6534498)
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(P813) Tuesday, October 15, 2019

(P1476) "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" (language: en)
(P248)
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(P813) Tuesday, October 15, 2019

(P2093) Shurtleff SA
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(P813) Tuesday, October 15, 2019

Buijs A
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Behm FG
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Rubnitz JE
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Raimondi SC
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Hancock ML
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Pui CH
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Grosveld G
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Downing JR
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description scientific article published on 01 December 1995

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