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ArticleHuman mutation2013

Genetic abnormalities in FOXP1 are associated with congenital heart defects.

Sheng-Wei Chang et al.PubMed ↗Full text ↗Publisher ↗

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37 papers cite it

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this papertrialcites it

2 trials

NCT011920485,000 enrolled2009NCT0621167325 enrolled2024
Full record →Abstract, authors, funding and every citing paper · PMID 23766104