Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel

Documenti analoghi

• A comprehensive targeted next‐generation sequencing panel for genetic diagnosis of patients with suspected inherited thrombocytopenia
  di: Johnson, Ben, et al.
  Pubblicazione: (2018)
• Results of next‐generation sequencing gene panel diagnostics including copy‐number variation analysis in 810 patients suspected of heritable thoracic aortic disorders
  di: Overwater, Eline, et al.
  Pubblicazione: (2018)
• Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects
  di: Stockley, Jacqueline, et al.
  Pubblicazione: (2013)
• SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects
  di: Fletcher, Sarah J., et al.
  Pubblicazione: (2015)
• Evaluation of a whole blood remote platelet function test for the diagnosis of mild bleeding disorders
  di: Dovlatova, Natalia, et al.
  Pubblicazione: (2014)