APA (7th ed.) Citation

Nematollahi, S., Hamdy, R. C., van Bosse, H., Li, J., Blanshay‐Goldberg, D., de Vries, J. I. P., . . . Dahan‐Oliel, N. (2025). Human Phenotype Ontology Annotations for Rare Congenital Conditions: Application to Arthrogryposis Multiplex Congenita. American Journal of Medical Genetics. Part A, 197(8), 1. https://doi.org/10.1002/ajmg.a.64067

Chicago Style (17th ed.) Citation

Nematollahi, Shahrzad, et al. "Human Phenotype Ontology Annotations for Rare Congenital Conditions: Application to Arthrogryposis Multiplex Congenita." American Journal of Medical Genetics. Part A 197, no. 8 (2025): 1. https://doi.org/10.1002/ajmg.a.64067.

MLA (9th ed.) Citation

Nematollahi, Shahrzad, et al. "Human Phenotype Ontology Annotations for Rare Congenital Conditions: Application to Arthrogryposis Multiplex Congenita." American Journal of Medical Genetics. Part A, vol. 197, no. 8, 2025, p. 1, https://doi.org/10.1002/ajmg.a.64067.