(Q40393824)
Statements
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Novel RET mutation produces a truncated RET receptor lacking the intracellular signaling domain in a 3-generation family with Hirschsprung disease (English)
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Vincent C H Lui
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Thomas Y Y Leon
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Maria-Mercedes Garcia-Barceló
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Raymond W Ganster
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Benedict L S Chen
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John M Hutson
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Paul K H Tam
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1 August 2005
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51
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8
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1552-1554
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Identifiers
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