Clinicians’ views and experiences with offering and returning results from exome sequencing to parents of infants with hearing loss by Notini, L, Gaff, CL, Savulescu, J, Vears, DF

Are We Ready for Whole Population Genomic Sequencing of Asymptomatic Newborns? by Vears DF, Savulescu J, Christodoulou J, Wall M, Newson AJ

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Are we ready for whole population genomic sequencing of asymptomatic newborns? by Vears, DF, Savulescu, J, Christodoulou, J, Wall, M, Newson, AJ

Australian public perspectives on genomic newborn screening: which conditions should be included? by Lynch, F, Best, S, Gaff, C, Downie, L, Archibald, AD, Gyngell, C, Goranitis, I, Peters, R, Savulescu, J, Lunke, S, Stark, Z, Vears, DF