Concepedia

Fluorescence in situ hybridization analysis of the cryptic t(12;21) (p13;q22) in childhood B-lineage acute lymphoblastic leukemia

Orly Yehuda-Gafni, Gabriel Cividalli, Ayala Abrahmov, Michael Weintrob, Susana Ben Neriah, Rachel E. Cohen, Dvorah Abeliovich

Cancer Genetics and Cytogenetics · 2002 · 14 citations · 16 references

DOI

Concepts

References

16

Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia.

Todd R. Golub, G. F. Barker, Stefan K. Bohlander et al. · Proceedings of the National Academy of Sciences · 1995 · 719 citations

, , +17

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.

Sheila Shurtleff, Arjan Buijs, F G Behm et al. · PubMed · 1995 · 561 citations

, , +9

High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia

Healegne Poirel, M Leconiat, MA Flexor et al. · Blood · 1995 · 442 citations · Full text

, , +11

TEL/AML-1 dimerizes and is associated with a favorable outcome in childhood acute lymphoblastic leukemia

TW McLean, Sarah Ringold, Donna Neuberg et al. · Blood · 1996 · 296 citations · Full text

, , +12

TEL/AML-1 dimerizes and is associated with a favorable outcome in childhood acute lymphoblastic leukemia

TW McLean, Sarah Ringold, Donna Neuberg et al. · Blood · 1996 · 236 citations

, , +12