APA (7th ed.) Citation

CP, B., A, C., P, C., CP, R., & RV, T. (2005). A family with autosomal dominant hypocalcaemia with hypercalciuria (ADHH): Mutational analysis, phenotypic variability and treatment challenges. Journal of pediatric endocrinology & metabolism : JPEM, 18(7), 689. https://doi.org/10.1515/jpem.2005.18.7.689

Chicago Style (17th ed.) Citation

CP, Burren, Curley A, Christie P, Rodda CP, and Thakker RV. "A Family with Autosomal Dominant Hypocalcaemia with Hypercalciuria (ADHH): Mutational Analysis, Phenotypic Variability and Treatment Challenges." Journal of Pediatric Endocrinology & Metabolism : JPEM 18, no. 7 (2005): 689. https://doi.org/10.1515/jpem.2005.18.7.689.

MLA (9th ed.) Citation

CP, Burren, et al. "A Family with Autosomal Dominant Hypocalcaemia with Hypercalciuria (ADHH): Mutational Analysis, Phenotypic Variability and Treatment Challenges." Journal of Pediatric Endocrinology & Metabolism : JPEM, vol. 18, no. 7, 2005, p. 689, https://doi.org/10.1515/jpem.2005.18.7.689.