APA citiranje

Goos, J. A., Fenwick, A. L., Swagemakers, S. M., McGowan, S. J., Knight, S. J., Twigg, S. R., . . . van den Ouweland, A. M. (2016). Identification of Intragenic Exon Deletions and Duplication of TCF12 by Whole Genome or Targeted Sequencing as a Cause of TCF12‐Related Craniosynostosis. Hum Mutat.

Citação norma Chicago

Goos, Jacqueline A.C., et al. "Identification of Intragenic Exon Deletions and Duplication of TCF12 By Whole Genome or Targeted Sequencing As a Cause of TCF12‐Related Craniosynostosis." Hum Mutat 2016.

MLA citiranje

Goos, Jacqueline A.C., et al. "Identification of Intragenic Exon Deletions and Duplication of TCF12 By Whole Genome or Targeted Sequencing As a Cause of TCF12‐Related Craniosynostosis." Hum Mutat 2016.