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

Benzer Materyaller

• 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
  Yazar:: Webber, C, ve diğerleri
  Baskı/Yayın Bilgisi: (2010)
• Forging links between human mental retardation-associated CNVs and mouse gene knockout models.
  Yazar:: Webber, C, ve diğerleri
  Baskı/Yayın Bilgisi: (2009)
• Accurate distinction of pathogenic from benign CNVs in mental retardation.
  Yazar:: Hehir-Kwa, J, ve diğerleri
  Baskı/Yayın Bilgisi: (2010)
• Forging links between human mental retardation-associated CNVs and mouse gene knockout models.
  Yazar:: Caleb Webber, ve diğerleri
  Baskı/Yayın Bilgisi: (2009-06-01)
• Analysis of parental origin of de novo pathogenic CNVs in patients with intellectual disability
  Yazar:: Samara Socorro Silva Pereira, ve diğerleri
  Baskı/Yayın Bilgisi: (2024-08-01)