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

Podobne zapisy

• De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome
  od: Vetrini, Francesco, i wsp.
  Wydane: (2019)
• Behavior and Sleep Disturbance in Smith-Magenis Syndrome
  od: Shayota, Brian J., i wsp.
  Wydane: (2019)
• Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndrome.
  od: Elsea, S H, i wsp.
  Wydane: (1995)
• RAI1 variations in Smith–Magenis syndrome patients without 17p11.2 deletions
  od: Girirajan, S, i wsp.
  Wydane: (2005)
• Frameshift mutation hotspot identified in Smith-Magenis syndrome: case report and review of literature
  od: Truong, Hoa T, i wsp.
  Wydane: (2010)