APA (7e ed.) Bronvermelding

Whyte, M., Christie, P., Podgornik, M., Dixon, P., Eddy, M., Wooding, C., . . . Thakker, R. (1999). X-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotype.

Chicago (17e ed.) Bronvermelding

Whyte, M., et al. X-linked Hypophosphatemia (XLH): Mutations Compromising PHEX Structure Reflect a Severe Phenotype. 1999.

MLA (9e ed.) Bronvermelding

Whyte, M., et al. X-linked Hypophosphatemia (XLH): Mutations Compromising PHEX Structure Reflect a Severe Phenotype. 1999.