Cite

    Armes, J. E., Williams, M., Price, G., Wallis, T., Gallagher, R., Matsika, A., Joy, C., Galea, M., Gardener, G., Leach, R., Swagemakers, S. M., Tearle, R., Stubbs, A., Harraway, J., van der Spek, P. J., & Venter, D. J. (2018). application of Whole Genome Sequencing Technology in the Investigation of Genetic Causes of Fetal, Perinatal, and Early Infant Death. Pediatric and developmental pathology, 21, 54–67. http://access.bl.uk/ark:/81055/vdc_100070902106.0x000024