P623: BeginNGS: Nest digital genetics navigator facilitates scale while preserving participant experience and education

Lignende værker

• P623: BeginNGS: Nest digital genetics navigator facilitates scale while preserving participant experience and education
  af: Brandan Schultz, et al.
  Udgivet: (2025-01-01)
• Clinical utility and cost-effectiveness of BeginNGS newborn screening by genome sequencing and standard newborn screening for severe childhood genetic diseases: an adaptive, international and comparative clinical trial
  af: Lucia Guidugli, et al.
  Udgivet: (2025-11-01)
• P156: Genomic disease contribution for unknown causes of infant mortality via genome sequencing of newborn dried blood spots and semiautomated interpretation*
  af: Eric Ontiveros, et al.
  Udgivet: (2024-01-01)
• P470: A novel inherited frameshifting variant in UBA2 gene: A case study of highly variable phenotype in a family
  af: Kanika Parashar, et al.
  Udgivet: (2024-01-01)
• P610: Identification of trinucleotide repeat expansions in DMPK using rapid whole genome sequencing
  af: Lucia Guidugli, et al.
  Udgivet: (2024-01-01)