P164: Scalable Bayesian variant interpretation of Lynch syndrome genes using genotype and phenotype data for over 1.5M patients referred for testing*

Lignende værker

• P164: Scalable Bayesian variant interpretation of Lynch syndrome genes using genotype and phenotype data for over 1.5M patients referred for testing*
  af: Toby Manders, et al.
  Udgivet: (2024-01-01)
• P244: Developing Bayesian graphical models to provide continuous, probabilistic variant interpretation
  af: Toby Manders, et al.
  Udgivet: (2023-01-01)
• Phenotype-driven protocol switching is associated with improved ART outcomes under constant gonadotropin dosage: a self-controlled analysis of 4,632 cycles
  af: Jie Gao, et al.
  Udgivet: (2026-05-01)
• P216: Phenotype and genotype of Vietnamese patients with X-linked adrenoleukodystrophy
  af: Dung Vu, et al.
  Udgivet: (2024-01-01)
• P662: Updates on phenotypic spectrum and genotype-phenotype correlation of WDFY3-related syndrome
  af: Deqiong Ma, et al.
  Udgivet: (2024-01-01)