APA (7th ed.) Citation

Fenwick, A., Bowdin, S., Klatt, R., & Wilkie, A. (2011). A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome. BioMed Central.

Chicago Style (17th ed.) Citation

Fenwick, A., S. Bowdin, R. Klatt, and A. Wilkie. A Deletion of FGFR2 Creating a Chimeric IIIb/IIIc Exon in a Child with Apert Syndrome. BioMed Central, 2011.

MLA (9th ed.) Citation

Fenwick, A., et al. A Deletion of FGFR2 Creating a Chimeric IIIb/IIIc Exon in a Child with Apert Syndrome. BioMed Central, 2011.