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Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly

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Description scientific article published on 5 June 2008
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author: Maximilian Muenke  Felicitas Lacbawan  Jorge I Velez  Jeffrey A Towbin  John W. Belmont  Elizabeth Goldmuntz  Benjamin Feldman 

Publication date June 5, 2008
Language English
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