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FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly

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Description scientific article published on 28 June 2013
Author/s

author: Geert Mortier  Isabelle Migeotte  Guillaume Smits  Catheline Vilain  Guy Van Vliet 

Publication date June 28, 2013
Language English
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