Stephen, J., Vilboux, T., Mian, L., Kuptanon, C., Sinclair, C. M., Yildirimli, D., . . . Gunay-Aygun, M. (2017). Mutations in KIAA0753 cause Joubert syndrome associated with growth hormone deficiency. Hum Genet.
Citación estilo ChicagoStephen, Joshi, et al. "Mutations in KIAA0753 Cause Joubert Syndrome Associated With Growth Hormone Deficiency." Hum Genet 2017.
Cita MLAStephen, Joshi, et al. "Mutations in KIAA0753 Cause Joubert Syndrome Associated With Growth Hormone Deficiency." Hum Genet 2017.
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