High incidence of t(7;12)(q36;p13) in in
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Anne R. M. von Bergh; Ellen van Drunen; Elisabeth R. van Wering; Laura J. C. M.
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Article
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2006
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John Wiley and Sons
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English
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## Abstract The t(7;12)(q36;p13) is a recurrent translocation involving the __ETV6__/__TEL__ gene (12p13) and a heterogeneous breakpoint at 7q36. A fusion transcript between __HLXB9__ and __ETV6__ in AML with t(7;12) is occasionally found. To study the incidence of t(7;12) in infant and childhood a