Reply to Pembrey et al: ‘ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'

Lignende værker

• Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment
  af: Ceroni, Fabiola, et al.
  Udgivet: (2014)
• ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis
  af: Pembrey, Marcus, et al.
  Udgivet: (2015)
• ZNF277 regulates ovarian cancer cell proliferation and invasion through inhibition of PTEN
  af: Liu, Zhengling, et al.
  Udgivet: (2019)
• An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder
  af: Cameli, Cinzia, et al.
  Udgivet: (2021)
• Genome-wide analysis identifies a role for common copy number variants in specific language impairment
  af: Simpson, Nuala H, et al.
  Udgivet: (2015)