APA (7e ed.) Bronvermelding

Twigg, S., Kan, R., Babbs, C., Bochukova, E., Robertson, S., Wall, S., . . . Wilkie, A. (2004). Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome.

Chicago (17e ed.) Bronvermelding

Twigg, SR, R. Kan, C. Babbs, E. Bochukova, S. Robertson, SA Wall, G. Morriss-Kay, en A. Wilkie. Mutations of Ephrin-B1 (EFNB1), a Marker of Tissue Boundary Formation, Cause Craniofrontonasal Syndrome. 2004.

MLA (9e ed.) Bronvermelding

Twigg, SR, et al. Mutations of Ephrin-B1 (EFNB1), a Marker of Tissue Boundary Formation, Cause Craniofrontonasal Syndrome. 2004.