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Long JC, Pomare C, Best S, Boughtwood T, North K, Ellis LA, Churruca K, Braithwaite J. Building a learning community of Australian clinical genomics: a social network study of the Australian Genomic Health Alliance. BMC Medicine. 2019. 17 (1) : 44.
Gyngell, C., Newson, A.J., Wilkinson, D., Stark, Z., & Savulescu, J. (2019). Rapid Challenges: Ethics and Genomic Neonatal Intensive Care. Pediatrics, 143(Suppl 1), S14-s21.
Stark, Z., Dolman, L., Manolio, T.A., Ozenberger, B., Hill, S.L., Caulfied, M.J., et al. (2019). Integrating Genomics into Healthcare: A Global Responsibility. Am J Hum Genet, 104(1), 13-20.
Dillon OJ, Lunke S, Stark Z, Yeung A, Thorne N, Melbourne Genomics Health Alliance, et al. Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disorders. European Journal of Human Genetics. 2018. [Epub ahead of print]
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