APA (7th ed.) Citation

Loucks, C. M., Parboosingh, J. S., Shaheen, R., Bernier, F. P., McLeod, D. R., Seidahmed, M. Z., . . . Innes, A. M. (2015). Matching Two Independent Cohorts Validates DPH1 as a Gene Responsible for Autosomal Recessive Intellectual Disability with Short Stature, Craniofacial, and Ectodermal Anomalies. Human mutation, 36(10), 1015-1019. https://doi.org/10.1002/humu.22843

Chicago Style (17th ed.) Citation

Loucks, Catrina M., et al. "Matching Two Independent Cohorts Validates DPH1 as a Gene Responsible for Autosomal Recessive Intellectual Disability with Short Stature, Craniofacial, and Ectodermal Anomalies." Human Mutation 36, no. 10 (2015): 1015-1019. https://doi.org/10.1002/humu.22843.

MLA (9th ed.) Citation

Loucks, Catrina M., et al. "Matching Two Independent Cohorts Validates DPH1 as a Gene Responsible for Autosomal Recessive Intellectual Disability with Short Stature, Craniofacial, and Ectodermal Anomalies." Human Mutation, vol. 36, no. 10, 2015, pp. 1015-1019, https://doi.org/10.1002/humu.22843.