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Rapid genomic testing in critically ill patients with genetic conditions: position statement by the Human Genetics Society of Australasia.
European Journal of Human Genetics
32(2)
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2024
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Should secondary pharmacogenomic variants be actively screened and reported when diagnostic genome-wide sequencing is performed in a child?.
Genetics in Medicine
26(2)
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Return of individual research results from genomic research: A systematic review of stakeholder perspectives.
PLOS ONE
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Notini, L, Gaff, CL, Savulescu, J, Vears, DF.
Clinicians’ Views and Experiences with Offering and Returning Results from Exome Sequencing to Parents of Infants with Hearing Loss.
Journal of Clinical Medicine
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