https://www.selleckchem.com/pr....oducts/ag-120-Ivosid
Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a multifaceted syndrome with a variable phenotype. Few studies have described the associated dental characteristics and their relationship with medical co-morbidities; and no Australian data exist. To determine the clinical manifestations and correlations between oral and medical conditions in children with 22q11.2DS. A retrospective observational study. Children genetically diagnosed with 22q11.2DS at the Royal Children's Hospital Melbourne were selected; their medical and d
Like
Comment
Share
