P597: All for One Clinical Genomics Network: Linking Canadian diagnostic laboratories to share genome-wide sequencing data to support rare disease diagnosis

Antzeko izenburuak

• P616: Genome-wide Sequencing Ontario (GSO): Insight into Ontario’s rare disease landscape
  nork: Meredith Gillespie, et al.
  Argitaratua: (2024-01-01)
• P540: Genome-wide Sequencing Ontario (GSO): Canada’s first provincial clinical genome-wide sequencing service
  nork: Meredith Gillespie, et al.
  Argitaratua: (2024-01-01)
• O05: A micro-costing and cost-effectiveness analysis of genome sequencing vs exome sequencing in pediatric rare diseases
  nork: Wendy Ungar, et al.
  Argitaratua: (2024-01-01)
• P375: Case study: Germline chromoanagenesis associated with global developmental delay, dysmorphic features and failure to thrive
  nork: Priya Bhola, et al.
  Argitaratua: (2024-01-01)
• P740: DMD or not DMD? Clinical genome sequencing in the interpretation of complex copy number gains
  nork: Edward Higginbotham, et al.
  Argitaratua: (2024-01-01)