Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome

Ítems similars

• De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome
  per: Vetrini, Francesco, et al.
  Publicat: (2019)
• Behavior and Sleep Disturbance in Smith-Magenis Syndrome
  per: Shayota, Brian J., et al.
  Publicat: (2019)
• Smith-Magenis syndrome patients often display antibody deficiency but not other immune pathologies
  per: Perkins, Tiffany, et al.
  Publicat: (2017)
• Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndrome.
  per: Elsea, S H, et al.
  Publicat: (1995)
• RAI1 variations in Smith–Magenis syndrome patients without 17p11.2 deletions
  per: Girirajan, S, et al.
  Publicat: (2005)