Publication Angiographic diagnosis, prevalence and outcomes for left ventricular noncompaction in children with congenital cardiac disease.
Publication Building Better Communities for Children: Community implementation and evaluation of the Australian Early Development Index
Publication Coexistent MEFV and CIAS1 mutations manifesting as familial Mediterranean fever plus deafness.
Publication Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation.
Publication Delineation of large deletions of the MECP2 gene in Rett syndrome patients, including a familial case with a male proband.
Publication Estimating the prevalence of fetal alcohol syndrome in Victoria using routinely collected administrative data.
Publication Insulin-like growth factor-1 is not essential for the intestinal trophic effects of glucagon-like peptide-2.
Publication Interpreting missense variants: comparing computational methods in human disease genes CDKN2A, MLH1, MSH2, MECP2, and tyrosinase (TYR).
