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.
Dyfyniad Arddull ChicagoWhyte, M., et al. X-linked Hypophosphatemia (XLH): Mutations Compromising PHEX Structure Reflect a Severe Phenotype. 1999.
Dyfyniad MLAWhyte, M., et al. X-linked Hypophosphatemia (XLH): Mutations Compromising PHEX Structure Reflect a Severe Phenotype. 1999.
Rhybudd: Mae'n bosib nad yw'r dyfyniadau hyn bob amser yn 100% cywir.