Investigation of meiotic rearrangements in DGS/VCFS patients with a microdeletion 22q11.2

Lignende værker

• Atypical 22q11.2 deletion in a patient with DGS/VCFS spectrum
  af: Nogueira, Sintia Iole, et al.
  Udgivet: (2008)
• Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements
  af: Demaerel, Wolfram, et al.
  Udgivet: (2017)
• Retraction Notice to: Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements
  af: Demaerel, Wolfram, et al.
  Udgivet: (2018)
• 22q11.2 microdeletion syndrome as a multidisciplinary problem
  af: Marta Skoczyńska, et al.
  Udgivet: (2017-12-01)
• Microdeletion 22q11.2: clinical data and deletion size
  af: KERSTJENS-FREDERI..., W, et al.
  Udgivet: (1999)