Whyte, M. P., Christie, P. T., Podgornik, M. N., Dixon, P. H., Eddy, M. C., Wooding, C., Trump, D., Grieff, M., Mumm, S., Shlessinger, D., & Thakker, R. V. (1999). X-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotype. AMERICAN JOURNAL OF HUMAN GENETICS, 65(4), A114–A114.

Whyte, M. P., et al. “X-Linked Hypophosphatemia (XLH): Mutations Compromising PHEX Structure Reflect a Severe Phenotype.” AMERICAN JOURNAL OF HUMAN GENETICS, vol. 65, no. 4, 1999, pp. A114–A114.

Whyte, MP, PT Christie, MN Podgornik, PH Dixon, MC Eddy, C Wooding, D Trump, et al. 1999. “X-Linked Hypophosphatemia (XLH): Mutations Compromising PHEX Structure Reflect a Severe Phenotype.” AMERICAN JOURNAL OF HUMAN GENETICS 65 (4): A114–A114.