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Pediatric Dermatology|April 5, 2016
Pachyonychia Congenita: A Spectrum of KRT6a Mutations in Australian PatientsCharlotte E Forrest, Genevieve Casey, Dylan A Mordaunt, et al.
Australian Health Review : a Publication of the Australian Hospital Association|November 12, 2025
Navigating medication safety with electronic medical records: insights from a dual-phase implementation in paediatric, neonatal and maternity careDylan A Mordaunt, Nichola Johnson, Santosh Verghese, et al.
Archives of Rehabilitation Research and Clinical Translation|September 25, 2023
"The Days Are Long But the Nights Are Even Longer": A Mixed-Method Study of Sleep Disturbances Among Patients in an Inpatient Rehabilitation ProgramMiia Rahja, Kate Laver, Dylan A Mordaunt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 2, 2024
The cost of proband and trio exome and genome analysis in rare disease: A micro-costing studyDylan A Mordaunt, Francisco Santos Gonzalez, Sebastian Lunke, et al.
Systematic Reviews|April 9, 2024
Patient characteristics of, and remedial interventions for, complaints and medico-legal claims against doctors: a rapid review of the literatureTimothy J Schultz, Michael Zhou, Jodi Gray, et al.
American Journal of Medical Genetics. Part A|August 21, 2015
Presentation of m.3243A>G (MT-TL1; tRNALeu) variant with focal neurology in infancyDylan A Mordaunt, Liam C McIntyre, Hayley Salvemini, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Phenotypic variation of TTC19-deficient mitochondrial complex III deficiency: a case report and literature reviewDylan A Mordaunt, Alexandra Jolley, Shanti Balasubramaniam, et al.
NPJ Genomic Medicine|November 23, 2019
Identification and targeted management of a neurodegenerative disorder caused by biallelic mutations in SLC5A6Alicia B Byrne, Peer Arts, Steven W Polyak, et al.
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