Publication A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort.
Publication A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemia.
Publication Editorial comments on: "The burden of food allergy on children and teens: A systematic review".
Publication Identifying low-grade cellular rejection after heart transplantation in children by using gene expression profiling.
Publication Importance of accounting for sibling age when examining the association between family size and early childhood cognition, language and emotional behaviour: a birth cohort study.
