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APA Citation
Marshall, C., Farrell, S., Cushing, D., Paton, T., Stockley, T., Stavropoulos, D., Ray, P., Szego, M., Lau, L., Pereira, S., Cohn, R., Wintle, R., Abuzenadah, A., Abu-Elmagd, M., & Scherer, S. (2015). whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome. BMC genomics, 16, 1–7. http://access.bl.uk/ark:/81055/vdc_100080456416.0x00018f