A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome by Fenwick, A, Bowdin, S, Klatt, R, Wilkie, A

A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome. by Fenwick, A, Bowdin, S, Klatt, R, Wilkie, A