APA (7th ed.) Citation

Parsons, S. J. H., Wright, N. B., Burkitt‐Wright, E., Skae, M. S., & Murray, P. G. (2017). A heterozygous microdeletion of 20p12.2-3 encompassing PROKR2 and BMP2 in a patient with congenital hypopituitarism and growth hormone deficiency. American Journal of Medical Genetics. Part A, 173(8), 2261. https://doi.org/10.1002/ajmg.a.38306

Chicago Style (17th ed.) Citation

Parsons, Samuel J. H., Neville B. Wright, Emma Burkitt‐Wright, Mars S. Skae, and Phillip G. Murray. "A Heterozygous Microdeletion of 20p12.2-3 Encompassing PROKR2 and BMP2 in a Patient with Congenital Hypopituitarism and Growth Hormone Deficiency." American Journal of Medical Genetics. Part A 173, no. 8 (2017): 2261. https://doi.org/10.1002/ajmg.a.38306.

MLA (9th ed.) Citation

Parsons, Samuel J. H., et al. "A Heterozygous Microdeletion of 20p12.2-3 Encompassing PROKR2 and BMP2 in a Patient with Congenital Hypopituitarism and Growth Hormone Deficiency." American Journal of Medical Genetics. Part A, vol. 173, no. 8, 2017, p. 2261, https://doi.org/10.1002/ajmg.a.38306.