APA (7e ed.) Bronvermelding

Vasudevan, P., Twigg, S., Mulliken, J., Cook, J., Quarrell, O., & Wilkie, A. (2006). Expanding the phenotype of craniofrontonasal syndrome: Two unrelated boys with EFNB1 mutations and congenital diaphragmatic hernia.

Chicago (17e ed.) Bronvermelding

Vasudevan, P., SR Twigg, J. Mulliken, J. Cook, O. Quarrell, en A. Wilkie. Expanding the Phenotype of Craniofrontonasal Syndrome: Two Unrelated Boys with EFNB1 Mutations and Congenital Diaphragmatic Hernia. 2006.

MLA (9e ed.) Bronvermelding

Vasudevan, P., et al. Expanding the Phenotype of Craniofrontonasal Syndrome: Two Unrelated Boys with EFNB1 Mutations and Congenital Diaphragmatic Hernia. 2006.