Tell, S., Finn, E., Ohman-Hanson, R. A., & Ma, N. (2020). SUN-LB13 Idiopathic Infantile Hypercalcemia Secondary to CYP24A1 Mutation: A Rare Case Without Exogenous Vitamin D Supplementation. J Endocr Soc.
Styl ChicagoTell, Shoshana, Erin Finn, Rebecca Anne Ohman-Hanson, a Nina Ma. "SUN-LB13 Idiopathic Infantile Hypercalcemia Secondary to CYP24A1 Mutation: A Rare Case Without Exogenous Vitamin D Supplementation." J Endocr Soc 2020.
Citace podle MLATell, Shoshana, Erin Finn, Rebecca Anne Ohman-Hanson, a Nina Ma. "SUN-LB13 Idiopathic Infantile Hypercalcemia Secondary to CYP24A1 Mutation: A Rare Case Without Exogenous Vitamin D Supplementation." J Endocr Soc 2020.
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