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APA Citation
Stavropoulos, D. J., Marshall, C. R., Basran, R. K., Lau, L., Eliou, M., Orr, J., Liston, E. J., Bowdin, S., Meyn, M., Carter, M., Carew, C., Cohn, R. D., Shlien, A., & Ray, P. N. (n.d.). mG-130 Utilising whole exome sequencing to identify causative variants in genetically heterogeneous disorders. Journal of medical genetics, 52, A11. http://access.bl.uk/ark:/81055/vdc_100135162437.0x000042