HuGE Literature Finder
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Genetic abnormalities in FOXP1 are associated with congenital heart defects. Human mutation 2013 Sep 34 (9): 1226-30. Chang Sheng-Wei, Mislankar Mona, Misra Chaitali, Huang Nianyuan, Dajusta Daniel G, Harrison Steven M, McBride Kim L, Baker Linda A, Garg Vi |
- Page last reviewed:Feb 1, 2023
- Page last updated:Feb 03, 2023
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