Publication A mutation in MT-TW causes a tRNA processing defect and reduced mitochondrial function in a family with Leigh syndrome.
Publication Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene.
Publication Neonatal MRI is associated with future cognition and academic achievement in preterm children.
Publication Muscle weakness in TPM3-myopathy is due to reduced Ca2+-sensitivity and impaired acto-myosin cross-bridge cycling in slow fibres.
Publication All the World's a Stage: Facilitating Discovery Science and Improved Cancer Care through the Global Alliance for Genomics and Health.
Publication LINE-1 DNA methylation: A potential forensic marker for discriminating monozygotic twins.
Publication Language outcomes of children with cerebral palsy aged 5 years and 6 years: a population-based study.
Publication Detection of Neisseria gonorrhoeae in the pharynx and saliva: implications for gonorrhoea transmission.
Publication Parenting behavior at 2 years predicts school-age performance at 7 years in very preterm children.
Publication Outcomes of ventricular assist device implantation in children and young adults: the Melbourne experience.
