Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

Samankaltaisia teoksia

• Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease
  Tekijä: Sweeney, Nathaly M., et al.
  Julkaistu: (2021)
• Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease
  Tekijä: Sweeney, Nathaly M., et al.
  Julkaistu: (2021)
• The case for early use of rapid whole-genome sequencing in management of critically ill infants: late diagnosis of Coffin–Siris syndrome in an infant with left congenital diaphragmatic hernia, congenital heart disease, and recurrent infections
  Tekijä: Sweeney, Nathaly M., et al.
  Julkaistu: (2018)
• Rapid whole-genome sequencing identifies a novel homozygous NPC1 variant associated with Niemann–Pick type C1 disease in a 7-week-old male with cholestasis
  Tekijä: Hildreth, Amber, et al.
  Julkaistu: (2017)
• Rapid whole-genome sequencing identifies a novel GABRA1 variant associated with West syndrome
  Tekijä: Farnaes, Lauge, et al.
  Julkaistu: (2017)