P435: Diagnostic yield and copy number findings from 500 clinical genome sequencing cases

Lignende værker

• P435: Diagnostic yield and copy number findings from 500 clinical genome sequencing cases
  af: Kameryn Butler, et al.
  Udgivet: (2023-01-01)
• P582: Exon-level copy number variations identified by whole genome sequencing in previously undiagnosed patients with rare hereditary diseases
  af: Jiyong Wang, et al.
  Udgivet: (2023-01-01)
• Identification and analyses of exonic and copy number variants in spastic paraplegia
  af: Anum Shafique, et al.
  Udgivet: (2024-06-01)
• 17q25.3 copy number changes: association with neurodevelopmental disorders and cardiac malformation
  af: Nikhil Shri Sahajpal, et al.
  Udgivet: (2023-07-01)
• Copy Number Variants in Epileptic Encephalopathy
  af: J Gordon Millichap
  Udgivet: (2012-02-01)