P517: An automated approach to report drafting for newborn genomic sequencing in the BabySeq Project

Samankaltaisia teoksia

• P410: The effect of newborn genomic screening on downstream health care utilization and costs: Evidence from the BabySeq Project*
  Tekijä: Hadley Smith, et al.
  Julkaistu: (2023-01-01)
• Designing inclusive newborn sequencing research: insights from parents in underrepresented communities
  Tekijä: Maya C. del Rosario, et al.
  Julkaistu: (2026-01-01)
• Genetic counselors’ perspectives on genomic screening of apparently healthy newborns in the United States
  Tekijä: Maya C. del Rosario, et al.
  Julkaistu: (2024-01-01)
• P517: An automated approach to report drafting for newborn genomic sequencing in the BabySeq Project
  Tekijä: Anna Nagy, et al.
  Julkaistu: (2023-01-01)
• Parental Preferences for Expanded Newborn Screening: What Are the Limits?
  Tekijä: Nicole S. Y. Liang, et al.
  Julkaistu: (2023-08-01)