Ending the Diagnostic Odyssey: Is whole genome sequencing the answer?

Gelijkaardige items

• A homozygous mutation in PEX16 identified by whole-exome sequencing ending a diagnostic odyssey
  door: Bacino, Carlos A., et al.
  Gepubliceerd in: (2015)
• Utility of whole‐exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care
  door: Sawyer, S.L., et al.
  Gepubliceerd in: (2015)
• Whole-exome sequencing in neurologic practice: Reducing the diagnostic odyssey
  door: Johnson, Nicholas E.
  Gepubliceerd in: (2015)
• Pharmacogenomic findings from clinical whole exome sequencing of diagnostic odyssey patients
  door: Cousin, Margot A., et al.
  Gepubliceerd in: (2017)
• Whole exome sequencing in neurogenetic odysseys: An effective, cost- and time-saving diagnostic approach
  door: Córdoba, Marta, et al.
  Gepubliceerd in: (2018)