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Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants.

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Description scientific article published on October 2010
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author: Helen Griffin  Peter J Scambler  A. Graham Stuart  Christiane Zweier  John Burn  Judith A Goodship  John E. Deanfield  Anita Rauch 

Publication date October 1, 2010
Language English
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