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FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly
scientific article published on 28 June 2013
Author/s
author: Geert Mortier, Guillaume Smits, Isabelle Migeotte, Catheline Vilain, Guy Van Vliet
Work details
Publication date
June 28, 2013
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Language
English
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