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APA Citation
Le Quesne Stabej, P., James, C., Ocaka, L., Tekman, M., Grunewald, S., Clement, E., Stanescu, H., Kleta, R., Morrogh, D., Calder, A., Williams, H., & Bitner-Glindzicz, M. (2017). an example of the utility of genomic analysis for fast and accurate clinical diagnosis of complex rare phenotypes. Orphanet journal of rare diseases, 12(1), 1–8. http://access.bl.uk/ark:/81055/vdc_100081090444.0x000081