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-referens (17:e uppl.)Whyte, M., et al. X-linked Hypophosphatemia (XLH): Mutations Compromising PHEX Structure Reflect a Severe Phenotype. 1999.
MLA-referens (9:e uppl.)Whyte, M., et al. X-linked Hypophosphatemia (XLH): Mutations Compromising PHEX Structure Reflect a Severe Phenotype. 1999.
Varning: dessa hänvisningar är inte alltid fullständigt riktiga.