Fibroblast Growth Factor Receptor 2 and Its Role in Caudal Appendage and Craniosynostosis
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine,Otorhinolaryngology,Surgery
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3. Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer syndrome.;Piccione;Eur J Pediatr,2009
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