Dauber, A., Nguyen, T. T., Sochett, E., Cole, D. E. C., Horst, R., Abrams, S. A., . . . Hirschhorn, J. N. (2012). Genetic Defect in CYP24A1, the Vitamin D 24-Hydroxylase Gene, in a Patient with Severe Infantile Hypercalcemia. Endocrine Society.

Dauber, Andrew, Thutrang T. Nguyen, Etienne Sochett, David E. C. Cole, Ronald Horst, Steven A. Abrams, Thomas O. Carpenter, and Joel N. Hirschhorn. Genetic Defect in CYP24A1, the Vitamin D 24-Hydroxylase Gene, in a Patient With Severe Infantile Hypercalcemia. Endocrine Society, 2012.

Dauber, Andrew, et al. Genetic Defect in CYP24A1, the Vitamin D 24-Hydroxylase Gene, in a Patient With Severe Infantile Hypercalcemia. Endocrine Society, 2012.