A novel heterozygous mutation in FGFR2 gene causing Pfeiffer syndrome

Additional Supporting Information may be found online in the supporting information tab for this article. Figure S1. Images of the proband's mother Figure S2. Domains and 3D models analysis from native and mutant FGFR2 protein affecting the codon 290 in the literature Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.