Candidate genes and biological processes in de novo CNVs from autistic individuals

Ítems similars

• 46% of individuals with ASD that harbour de novo CNVs have at least one de novo CNV that overlaps a gene associated with synaptic signalling
  per: Webber, C, et al.
  Publicat: (2010)
• Forging links between human mental retardation-associated CNVs and mouse gene knockout models.
  per: Webber, C, et al.
  Publicat: (2009)
• Accurate distinction of pathogenic from benign CNVs in mental retardation.
  per: Hehir-Kwa, J, et al.
  Publicat: (2010)
• Analysis of parental origin of de novo pathogenic CNVs in patients with intellectual disability
  per: Samara Socorro Silva Pereira, et al.
  Publicat: (2024-08-01)
• Network topologies and convergent aetiologies arising from deletions and duplications observed in individuals with autism
  per: Noh, H, et al.
  Publicat: (2013)