APA (7th ed.) Citation

Rump, P., Jazayeri, O., van Dijk-Bos, K. K., Johansson, L. F., van Essen, A. J., Verheij, J. B. G. M., . . . Sikkema-Raddatz, B. (2016). Whole-exome sequencing is a powerful approach for establishing the etiological diagnosis in patients with intellectual disability and microcephaly. BMC Medical Genomics, 1. https://doi.org/10.1186/s12920-016-0167-8

Chicago Style (17th ed.) Citation

Rump, Patrick, et al. "Whole-exome Sequencing Is a Powerful Approach for Establishing the Etiological Diagnosis in Patients with Intellectual Disability and Microcephaly." BMC Medical Genomics 2016: 1. https://doi.org/10.1186/s12920-016-0167-8.

MLA (9th ed.) Citation

Rump, Patrick, et al. "Whole-exome Sequencing Is a Powerful Approach for Establishing the Etiological Diagnosis in Patients with Intellectual Disability and Microcephaly." BMC Medical Genomics, 2016, p. 1, https://doi.org/10.1186/s12920-016-0167-8.