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.
Čikaški stil citiranja (17. izdanje)Whyte, M., et al. X-linked Hypophosphatemia (XLH): Mutations Compromising PHEX Structure Reflect a Severe Phenotype. 1999.
MLA način citiranja (9. izdanje)Whyte, M., et al. X-linked Hypophosphatemia (XLH): Mutations Compromising PHEX Structure Reflect a Severe Phenotype. 1999.
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