Publication A novel deletion-insertion mutation identified in exon 3 of FXN in two siblings with a severe Friedreich ataxia phenotype.
Publication Distribution of human papillomavirus genotypes in archival cervical tissue from women with cervical cancer in urban Sri Lanka
Publication A population-based study and systematic review of hearing loss in children with cerebral palsy.
Publication Integrated genomic analysis of relapsed childhood acute lymphoblastic leukemia reveals therapeutic strategies
Publication Dysfunction of axonal membrane conductances in adolescents and young adults with spinal muscular atrophy
Publication Neonatal white matter abnormality predicts childhood motor impairment in very preterm children
