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 Style (17th ed.) CitationWhyte, M., et al. X-linked Hypophosphatemia (XLH): Mutations Compromising PHEX Structure Reflect a Severe Phenotype. 1999.
MLA (9th ed.) CitationWhyte, M., et al. X-linked Hypophosphatemia (XLH): Mutations Compromising PHEX Structure Reflect a Severe Phenotype. 1999.
Warning: These citations may not always be 100% accurate.